Ontology type: schema:ScholarlyArticle
1993-02
AUTHORSHerman J. Woerdenbag, Jos F. J. Lüers, Wim van Uden, Niesko Pras, Theo M. Malingré, A. Wilhelm Alfermann
ABSTRACTFrom aseptically grown Artemisia annua plantlets, shoot cultures were initiated. Using different concentrations of auxine, cytokinine and sucrose, a suitable culture medium was developed, with respect to the growth of the shoots and their artemisinin accumulation. Nitrate concentration and conductivity appeared to be suitable growth parameters. The artemisinin content was measured gas chromatographically. The shoot cultures were maintained in the developed standard medium, consisting of a half concentration of MS-salts with vitamins, 0.2 mg l-1 BAP, 0.05 mg l-1 NAA and 1% sucrose. The growth of the shoots and the artemisinin content remained stable for a longer period. They showed considerable photosynthetic activity and generally contained ca. 0.08% artemisinin on a dry weight basis. The highest artemisinin content found was 0.16% in the above mentioned standard medium, but also on the same medium with 0.5% sucrose. Attempts were made to further improve the artemisinin production by varying the medium composition through addition of gibberellic acid or casein hydroly-state; by omitting plant growth regulators; by precursor feeding, i.e. mevalonic acid; by influencing the biosynthesis routing through inhibition of the sterol synthesis by miconazole, naftifine or terbinafine; by changing gene expression with 5-azacytidine or colchicine; and by elicitation, using cellulase, chitosan, glutathione or nigeran. Enhanced artemisinin production was found with 10 mg l-1 gibberellic acid, 0.5 g l-1 casein hydrolysate, 10 mg l-1 or 20 mg l-1 naftifine. Relative increases of 154%, 169%, 140% and 120% were found, respectively. Other additions caused the growth to cease and the artemisinin contents to drop. More... »
PAGES247-257
http://scigraph.springernature.com/pub.10.1007/bf00029850
DOIhttp://dx.doi.org/10.1007/bf00029850
DIMENSIONShttps://app.dimensions.ai/details/publication/pub.1012709986
JSON-LD is the canonical representation for SciGraph data.
TIP: You can open this SciGraph record using an external JSON-LD service: JSON-LD Playground Google SDTT
[
{
"@context": "https://springernature.github.io/scigraph/jsonld/sgcontext.json",
"about": [
{
"id": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/06",
"inDefinedTermSet": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/",
"name": "Biological Sciences",
"type": "DefinedTerm"
},
{
"id": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/0607",
"inDefinedTermSet": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/",
"name": "Plant Biology",
"type": "DefinedTerm"
}
],
"author": [
{
"affiliation": {
"alternateName": "Department of Pharmacognosy, University Centre for Pharmacy, University of Groningen, A. Deusinglaan 2, NL-9713 AW, Groningen, The Netherlands",
"id": "http://www.grid.ac/institutes/grid.4830.f",
"name": [
"Department of Pharmacognosy, University Centre for Pharmacy, University of Groningen, A. Deusinglaan 2, NL-9713 AW, Groningen, The Netherlands"
],
"type": "Organization"
},
"familyName": "Woerdenbag",
"givenName": "Herman J.",
"id": "sg:person.010571302037.63",
"sameAs": [
"https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.010571302037.63"
],
"type": "Person"
},
{
"affiliation": {
"alternateName": "Department of Pharmacognosy, University Centre for Pharmacy, University of Groningen, A. Deusinglaan 2, NL-9713 AW, Groningen, The Netherlands",
"id": "http://www.grid.ac/institutes/grid.4830.f",
"name": [
"Department of Pharmacognosy, University Centre for Pharmacy, University of Groningen, A. Deusinglaan 2, NL-9713 AW, Groningen, The Netherlands"
],
"type": "Organization"
},
"familyName": "L\u00fcers",
"givenName": "Jos F. J.",
"id": "sg:person.012517047111.70",
"sameAs": [
"https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.012517047111.70"
],
"type": "Person"
},
{
"affiliation": {
"alternateName": "Department of Pharmacognosy, University Centre for Pharmacy, University of Groningen, A. Deusinglaan 2, NL-9713 AW, Groningen, The Netherlands",
"id": "http://www.grid.ac/institutes/grid.4830.f",
"name": [
"Department of Pharmacognosy, University Centre for Pharmacy, University of Groningen, A. Deusinglaan 2, NL-9713 AW, Groningen, The Netherlands"
],
"type": "Organization"
},
"familyName": "van Uden",
"givenName": "Wim",
"id": "sg:person.0711626754.06",
"sameAs": [
"https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.0711626754.06"
],
"type": "Person"
},
{
"affiliation": {
"alternateName": "Department of Pharmacognosy, University Centre for Pharmacy, University of Groningen, A. Deusinglaan 2, NL-9713 AW, Groningen, The Netherlands",
"id": "http://www.grid.ac/institutes/grid.4830.f",
"name": [
"Department of Pharmacognosy, University Centre for Pharmacy, University of Groningen, A. Deusinglaan 2, NL-9713 AW, Groningen, The Netherlands"
],
"type": "Organization"
},
"familyName": "Pras",
"givenName": "Niesko",
"id": "sg:person.01216512627.16",
"sameAs": [
"https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.01216512627.16"
],
"type": "Person"
},
{
"affiliation": {
"alternateName": "Department of Pharmacognosy, University Centre for Pharmacy, University of Groningen, A. Deusinglaan 2, NL-9713 AW, Groningen, The Netherlands",
"id": "http://www.grid.ac/institutes/grid.4830.f",
"name": [
"Department of Pharmacognosy, University Centre for Pharmacy, University of Groningen, A. Deusinglaan 2, NL-9713 AW, Groningen, The Netherlands"
],
"type": "Organization"
},
"familyName": "Malingr\u00e9",
"givenName": "Theo M.",
"id": "sg:person.016471320324.61",
"sameAs": [
"https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.016471320324.61"
],
"type": "Person"
},
{
"affiliation": {
"alternateName": "Institut f\u00fcr Entwicklungs- und Molekularbiologie der Pflanzen, Heinrich-Heine-Universit\u00e4t, Universit\u00e4tsstra\u00dfe 1, D-4000, D\u00fcsseldorf 1, Germany",
"id": "http://www.grid.ac/institutes/grid.411327.2",
"name": [
"Institut f\u00fcr Entwicklungs- und Molekularbiologie der Pflanzen, Heinrich-Heine-Universit\u00e4t, Universit\u00e4tsstra\u00dfe 1, D-4000, D\u00fcsseldorf 1, Germany"
],
"type": "Organization"
},
"familyName": "Alfermann",
"givenName": "A. Wilhelm",
"id": "sg:person.0642534353.59",
"sameAs": [
"https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.0642534353.59"
],
"type": "Person"
}
],
"citation": [
{
"id": "sg:pub.10.1007/bf00270085",
"sameAs": [
"https://app.dimensions.ai/details/publication/pub.1000592241",
"https://doi.org/10.1007/bf00270085"
],
"type": "CreativeWork"
},
{
"id": "sg:pub.10.1007/bf00033436",
"sameAs": [
"https://app.dimensions.ai/details/publication/pub.1035821842",
"https://doi.org/10.1007/bf00033436"
],
"type": "CreativeWork"
},
{
"id": "sg:pub.10.1007/bf01980041",
"sameAs": [
"https://app.dimensions.ai/details/publication/pub.1024730805",
"https://doi.org/10.1007/bf01980041"
],
"type": "CreativeWork"
},
{
"id": "sg:pub.10.1007/bf00040346",
"sameAs": [
"https://app.dimensions.ai/details/publication/pub.1030552004",
"https://doi.org/10.1007/bf00040346"
],
"type": "CreativeWork"
}
],
"datePublished": "1993-02",
"datePublishedReg": "1993-02-01",
"description": "From aseptically grown Artemisia annua plantlets, shoot cultures were initiated. Using different concentrations of auxine, cytokinine and sucrose, a suitable culture medium was developed, with respect to the growth of the shoots and their artemisinin accumulation. Nitrate concentration and conductivity appeared to be suitable growth parameters. The artemisinin content was measured gas chromatographically. The shoot cultures were maintained in the developed standard medium, consisting of a half concentration of MS-salts with vitamins, 0.2 mg l-1 BAP, 0.05 mg l-1 NAA and 1% sucrose. The growth of the shoots and the artemisinin content remained stable for a longer period. They showed considerable photosynthetic activity and generally contained ca. 0.08% artemisinin on a dry weight basis. The highest artemisinin content found was 0.16% in the above mentioned standard medium, but also on the same medium with 0.5% sucrose. Attempts were made to further improve the artemisinin production by varying the medium composition through addition of gibberellic acid or casein hydroly-state; by omitting plant growth regulators; by precursor feeding, i.e. mevalonic acid; by influencing the biosynthesis routing through inhibition of the sterol synthesis by miconazole, naftifine or terbinafine; by changing gene expression with 5-azacytidine or colchicine; and by elicitation, using cellulase, chitosan, glutathione or nigeran. Enhanced artemisinin production was found with 10 mg l-1 gibberellic acid, 0.5 g l-1 casein hydrolysate, 10 mg l-1 or 20 mg l-1 naftifine. Relative increases of 154%, 169%, 140% and 120% were found, respectively. Other additions caused the growth to cease and the artemisinin contents to drop.",
"genre": "article",
"id": "sg:pub.10.1007/bf00029850",
"inLanguage": "en",
"isAccessibleForFree": false,
"isPartOf": [
{
"id": "sg:journal.1123614",
"issn": [
"0167-6857",
"1573-5044"
],
"name": "Plant Cell, Tissue and Organ Culture (PCTOC)",
"publisher": "Springer Nature",
"type": "Periodical"
},
{
"issueNumber": "2",
"type": "PublicationIssue"
},
{
"type": "PublicationVolume",
"volumeNumber": "32"
}
],
"keywords": [
"artemisinin content",
"artemisinin production",
"shoot cultures",
"gibberellic acid",
"plant growth regulators",
"high artemisinin content",
"photosynthetic activity",
"gene expression",
"standard medium",
"growth regulators",
"Artemisia annua L.",
"artemisinin accumulation",
"antimalarial drug artemisinin",
"annua L.",
"precursor feeding",
"drug artemisinin",
"dry weight basis",
"shoots",
"growth parameters",
"sterol synthesis",
"same medium",
"culture medium",
"half concentration",
"suitable culture medium",
"medium composition",
"casein hydrolysate",
"growth",
"biosynthesis",
"cytokinine",
"plantlets",
"sucrose",
"weight basis",
"regulator",
"auxines",
"production",
"acid",
"L.",
"culture",
"cellulase",
"expression",
"nitrate concentrations",
"BAP",
"accumulation",
"artemisinin",
"glutathione",
"different concentrations",
"NAA",
"inhibition",
"medium",
"hydrolysate",
"feeding",
"nigeran",
"content",
"relative increase",
"suitable growth parameters",
"colchicine",
"activity",
"addition",
"long period",
"concentration",
"composition",
"synthesis",
"Ca",
"basis",
"vitamin",
"elicitation",
"increase",
"miconazole",
"terbinafine",
"attempt",
"respect",
"period",
"chitosan",
"parameters",
"naftifine",
"gas",
"conductivity",
"Artemisia annua plantlets"
],
"name": "Production of the new antimalarial drug artemisinin in shoot cultures of Artemisia annua L.",
"pagination": "247-257",
"productId": [
{
"name": "dimensions_id",
"type": "PropertyValue",
"value": [
"pub.1012709986"
]
},
{
"name": "doi",
"type": "PropertyValue",
"value": [
"10.1007/bf00029850"
]
}
],
"sameAs": [
"https://doi.org/10.1007/bf00029850",
"https://app.dimensions.ai/details/publication/pub.1012709986"
],
"sdDataset": "articles",
"sdDatePublished": "2022-06-01T22:01",
"sdLicense": "https://scigraph.springernature.com/explorer/license/",
"sdPublisher": {
"name": "Springer Nature - SN SciGraph project",
"type": "Organization"
},
"sdSource": "s3://com-springernature-scigraph/baseset/20220601/entities/gbq_results/article/article_225.jsonl",
"type": "ScholarlyArticle",
"url": "https://doi.org/10.1007/bf00029850"
}
]
Download the RDF metadata as: json-ld nt turtle xml License info
JSON-LD is a popular format for linked data which is fully compatible with JSON.
curl -H 'Accept: application/ld+json' 'https://scigraph.springernature.com/pub.10.1007/bf00029850'
N-Triples is a line-based linked data format ideal for batch operations.
curl -H 'Accept: application/n-triples' 'https://scigraph.springernature.com/pub.10.1007/bf00029850'
Turtle is a human-readable linked data format.
curl -H 'Accept: text/turtle' 'https://scigraph.springernature.com/pub.10.1007/bf00029850'
RDF/XML is a standard XML format for linked data.
curl -H 'Accept: application/rdf+xml' 'https://scigraph.springernature.com/pub.10.1007/bf00029850'
This table displays all metadata directly associated to this object as RDF triples.
190 TRIPLES
22 PREDICATES
108 URIs
96 LITERALS
6 BLANK NODES
Subject | Predicate | Object | |
---|---|---|---|
1 | sg:pub.10.1007/bf00029850 | schema:about | anzsrc-for:06 |
2 | ″ | ″ | anzsrc-for:0607 |
3 | ″ | schema:author | Nc4a9c3cbaea7469091ed7a09d92a084d |
4 | ″ | schema:citation | sg:pub.10.1007/bf00033436 |
5 | ″ | ″ | sg:pub.10.1007/bf00040346 |
6 | ″ | ″ | sg:pub.10.1007/bf00270085 |
7 | ″ | ″ | sg:pub.10.1007/bf01980041 |
8 | ″ | schema:datePublished | 1993-02 |
9 | ″ | schema:datePublishedReg | 1993-02-01 |
10 | ″ | schema:description | From aseptically grown Artemisia annua plantlets, shoot cultures were initiated. Using different concentrations of auxine, cytokinine and sucrose, a suitable culture medium was developed, with respect to the growth of the shoots and their artemisinin accumulation. Nitrate concentration and conductivity appeared to be suitable growth parameters. The artemisinin content was measured gas chromatographically. The shoot cultures were maintained in the developed standard medium, consisting of a half concentration of MS-salts with vitamins, 0.2 mg l-1 BAP, 0.05 mg l-1 NAA and 1% sucrose. The growth of the shoots and the artemisinin content remained stable for a longer period. They showed considerable photosynthetic activity and generally contained ca. 0.08% artemisinin on a dry weight basis. The highest artemisinin content found was 0.16% in the above mentioned standard medium, but also on the same medium with 0.5% sucrose. Attempts were made to further improve the artemisinin production by varying the medium composition through addition of gibberellic acid or casein hydroly-state; by omitting plant growth regulators; by precursor feeding, i.e. mevalonic acid; by influencing the biosynthesis routing through inhibition of the sterol synthesis by miconazole, naftifine or terbinafine; by changing gene expression with 5-azacytidine or colchicine; and by elicitation, using cellulase, chitosan, glutathione or nigeran. Enhanced artemisinin production was found with 10 mg l-1 gibberellic acid, 0.5 g l-1 casein hydrolysate, 10 mg l-1 or 20 mg l-1 naftifine. Relative increases of 154%, 169%, 140% and 120% were found, respectively. Other additions caused the growth to cease and the artemisinin contents to drop. |
11 | ″ | schema:genre | article |
12 | ″ | schema:inLanguage | en |
13 | ″ | schema:isAccessibleForFree | false |
14 | ″ | schema:isPartOf | N1d0367c4a45842fa81b6931b49f85a77 |
15 | ″ | ″ | N223fc538412745bbacc920c99a402ea9 |
16 | ″ | ″ | sg:journal.1123614 |
17 | ″ | schema:keywords | Artemisia annua L. |
18 | ″ | ″ | Artemisia annua plantlets |
19 | ″ | ″ | BAP |
20 | ″ | ″ | Ca |
21 | ″ | ″ | L. |
22 | ″ | ″ | NAA |
23 | ″ | ″ | accumulation |
24 | ″ | ″ | acid |
25 | ″ | ″ | activity |
26 | ″ | ″ | addition |
27 | ″ | ″ | annua L. |
28 | ″ | ″ | antimalarial drug artemisinin |
29 | ″ | ″ | artemisinin |
30 | ″ | ″ | artemisinin accumulation |
31 | ″ | ″ | artemisinin content |
32 | ″ | ″ | artemisinin production |
33 | ″ | ″ | attempt |
34 | ″ | ″ | auxines |
35 | ″ | ″ | basis |
36 | ″ | ″ | biosynthesis |
37 | ″ | ″ | casein hydrolysate |
38 | ″ | ″ | cellulase |
39 | ″ | ″ | chitosan |
40 | ″ | ″ | colchicine |
41 | ″ | ″ | composition |
42 | ″ | ″ | concentration |
43 | ″ | ″ | conductivity |
44 | ″ | ″ | content |
45 | ″ | ″ | culture |
46 | ″ | ″ | culture medium |
47 | ″ | ″ | cytokinine |
48 | ″ | ″ | different concentrations |
49 | ″ | ″ | drug artemisinin |
50 | ″ | ″ | dry weight basis |
51 | ″ | ″ | elicitation |
52 | ″ | ″ | expression |
53 | ″ | ″ | feeding |
54 | ″ | ″ | gas |
55 | ″ | ″ | gene expression |
56 | ″ | ″ | gibberellic acid |
57 | ″ | ″ | glutathione |
58 | ″ | ″ | growth |
59 | ″ | ″ | growth parameters |
60 | ″ | ″ | growth regulators |
61 | ″ | ″ | half concentration |
62 | ″ | ″ | high artemisinin content |
63 | ″ | ″ | hydrolysate |
64 | ″ | ″ | increase |
65 | ″ | ″ | inhibition |
66 | ″ | ″ | long period |
67 | ″ | ″ | medium |
68 | ″ | ″ | medium composition |
69 | ″ | ″ | miconazole |
70 | ″ | ″ | naftifine |
71 | ″ | ″ | nigeran |
72 | ″ | ″ | nitrate concentrations |
73 | ″ | ″ | parameters |
74 | ″ | ″ | period |
75 | ″ | ″ | photosynthetic activity |
76 | ″ | ″ | plant growth regulators |
77 | ″ | ″ | plantlets |
78 | ″ | ″ | precursor feeding |
79 | ″ | ″ | production |
80 | ″ | ″ | regulator |
81 | ″ | ″ | relative increase |
82 | ″ | ″ | respect |
83 | ″ | ″ | same medium |
84 | ″ | ″ | shoot cultures |
85 | ″ | ″ | shoots |
86 | ″ | ″ | standard medium |
87 | ″ | ″ | sterol synthesis |
88 | ″ | ″ | sucrose |
89 | ″ | ″ | suitable culture medium |
90 | ″ | ″ | suitable growth parameters |
91 | ″ | ″ | synthesis |
92 | ″ | ″ | terbinafine |
93 | ″ | ″ | vitamin |
94 | ″ | ″ | weight basis |
95 | ″ | schema:name | Production of the new antimalarial drug artemisinin in shoot cultures of Artemisia annua L. |
96 | ″ | schema:pagination | 247-257 |
97 | ″ | schema:productId | N09ee438e1db44b7ab193675ae63b4179 |
98 | ″ | ″ | N5e04625f47ea470fa3ef2a8445b55bb9 |
99 | ″ | schema:sameAs | https://app.dimensions.ai/details/publication/pub.1012709986 |
100 | ″ | ″ | https://doi.org/10.1007/bf00029850 |
101 | ″ | schema:sdDatePublished | 2022-06-01T22:01 |
102 | ″ | schema:sdLicense | https://scigraph.springernature.com/explorer/license/ |
103 | ″ | schema:sdPublisher | N1659217f6e604833a754d5d977ff4197 |
104 | ″ | schema:url | https://doi.org/10.1007/bf00029850 |
105 | ″ | sgo:license | sg:explorer/license/ |
106 | ″ | sgo:sdDataset | articles |
107 | ″ | rdf:type | schema:ScholarlyArticle |
108 | N068f8791275a4babbd622195927e0c2b | rdf:first | sg:person.0642534353.59 |
109 | ″ | rdf:rest | rdf:nil |
110 | N09ee438e1db44b7ab193675ae63b4179 | schema:name | doi |
111 | ″ | schema:value | 10.1007/bf00029850 |
112 | ″ | rdf:type | schema:PropertyValue |
113 | N1659217f6e604833a754d5d977ff4197 | schema:name | Springer Nature - SN SciGraph project |
114 | ″ | rdf:type | schema:Organization |
115 | N1d0367c4a45842fa81b6931b49f85a77 | schema:volumeNumber | 32 |
116 | ″ | rdf:type | schema:PublicationVolume |
117 | N223fc538412745bbacc920c99a402ea9 | schema:issueNumber | 2 |
118 | ″ | rdf:type | schema:PublicationIssue |
119 | N3b05398500e347dc9b8483925ec85cff | rdf:first | sg:person.0711626754.06 |
120 | ″ | rdf:rest | Nd351ddb03b4f4124817e01b8612c4ebd |
121 | N5e04625f47ea470fa3ef2a8445b55bb9 | schema:name | dimensions_id |
122 | ″ | schema:value | pub.1012709986 |
123 | ″ | rdf:type | schema:PropertyValue |
124 | N900137bf3e8b4bec81ecd37c3a137cd5 | rdf:first | sg:person.016471320324.61 |
125 | ″ | rdf:rest | N068f8791275a4babbd622195927e0c2b |
126 | Na91768696e3f4585928c8cbb153379ce | rdf:first | sg:person.012517047111.70 |
127 | ″ | rdf:rest | N3b05398500e347dc9b8483925ec85cff |
128 | Nc4a9c3cbaea7469091ed7a09d92a084d | rdf:first | sg:person.010571302037.63 |
129 | ″ | rdf:rest | Na91768696e3f4585928c8cbb153379ce |
130 | Nd351ddb03b4f4124817e01b8612c4ebd | rdf:first | sg:person.01216512627.16 |
131 | ″ | rdf:rest | N900137bf3e8b4bec81ecd37c3a137cd5 |
132 | anzsrc-for:06 | schema:inDefinedTermSet | anzsrc-for: |
133 | ″ | schema:name | Biological Sciences |
134 | ″ | rdf:type | schema:DefinedTerm |
135 | anzsrc-for:0607 | schema:inDefinedTermSet | anzsrc-for: |
136 | ″ | schema:name | Plant Biology |
137 | ″ | rdf:type | schema:DefinedTerm |
138 | sg:journal.1123614 | schema:issn | 0167-6857 |
139 | ″ | ″ | 1573-5044 |
140 | ″ | schema:name | Plant Cell, Tissue and Organ Culture (PCTOC) |
141 | ″ | schema:publisher | Springer Nature |
142 | ″ | rdf:type | schema:Periodical |
143 | sg:person.010571302037.63 | schema:affiliation | grid-institutes:grid.4830.f |
144 | ″ | schema:familyName | Woerdenbag |
145 | ″ | schema:givenName | Herman J. |
146 | ″ | schema:sameAs | https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.010571302037.63 |
147 | ″ | rdf:type | schema:Person |
148 | sg:person.01216512627.16 | schema:affiliation | grid-institutes:grid.4830.f |
149 | ″ | schema:familyName | Pras |
150 | ″ | schema:givenName | Niesko |
151 | ″ | schema:sameAs | https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.01216512627.16 |
152 | ″ | rdf:type | schema:Person |
153 | sg:person.012517047111.70 | schema:affiliation | grid-institutes:grid.4830.f |
154 | ″ | schema:familyName | Lüers |
155 | ″ | schema:givenName | Jos F. J. |
156 | ″ | schema:sameAs | https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.012517047111.70 |
157 | ″ | rdf:type | schema:Person |
158 | sg:person.016471320324.61 | schema:affiliation | grid-institutes:grid.4830.f |
159 | ″ | schema:familyName | Malingré |
160 | ″ | schema:givenName | Theo M. |
161 | ″ | schema:sameAs | https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.016471320324.61 |
162 | ″ | rdf:type | schema:Person |
163 | sg:person.0642534353.59 | schema:affiliation | grid-institutes:grid.411327.2 |
164 | ″ | schema:familyName | Alfermann |
165 | ″ | schema:givenName | A. Wilhelm |
166 | ″ | schema:sameAs | https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.0642534353.59 |
167 | ″ | rdf:type | schema:Person |
168 | sg:person.0711626754.06 | schema:affiliation | grid-institutes:grid.4830.f |
169 | ″ | schema:familyName | van Uden |
170 | ″ | schema:givenName | Wim |
171 | ″ | schema:sameAs | https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.0711626754.06 |
172 | ″ | rdf:type | schema:Person |
173 | sg:pub.10.1007/bf00033436 | schema:sameAs | https://app.dimensions.ai/details/publication/pub.1035821842 |
174 | ″ | ″ | https://doi.org/10.1007/bf00033436 |
175 | ″ | rdf:type | schema:CreativeWork |
176 | sg:pub.10.1007/bf00040346 | schema:sameAs | https://app.dimensions.ai/details/publication/pub.1030552004 |
177 | ″ | ″ | https://doi.org/10.1007/bf00040346 |
178 | ″ | rdf:type | schema:CreativeWork |
179 | sg:pub.10.1007/bf00270085 | schema:sameAs | https://app.dimensions.ai/details/publication/pub.1000592241 |
180 | ″ | ″ | https://doi.org/10.1007/bf00270085 |
181 | ″ | rdf:type | schema:CreativeWork |
182 | sg:pub.10.1007/bf01980041 | schema:sameAs | https://app.dimensions.ai/details/publication/pub.1024730805 |
183 | ″ | ″ | https://doi.org/10.1007/bf01980041 |
184 | ″ | rdf:type | schema:CreativeWork |
185 | grid-institutes:grid.411327.2 | schema:alternateName | Institut für Entwicklungs- und Molekularbiologie der Pflanzen, Heinrich-Heine-Universität, Universitätsstraße 1, D-4000, Düsseldorf 1, Germany |
186 | ″ | schema:name | Institut für Entwicklungs- und Molekularbiologie der Pflanzen, Heinrich-Heine-Universität, Universitätsstraße 1, D-4000, Düsseldorf 1, Germany |
187 | ″ | rdf:type | schema:Organization |
188 | grid-institutes:grid.4830.f | schema:alternateName | Department of Pharmacognosy, University Centre for Pharmacy, University of Groningen, A. Deusinglaan 2, NL-9713 AW, Groningen, The Netherlands |
189 | ″ | schema:name | Department of Pharmacognosy, University Centre for Pharmacy, University of Groningen, A. Deusinglaan 2, NL-9713 AW, Groningen, The Netherlands |
190 | ″ | rdf:type | schema:Organization |