@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP266714.RAyTIeVhT3SjJP0m--idEYB2sveW5YHA6sFoXGnHYEFpw
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP266714.RAyTIeVhT3SjJP0m--idEYB2sveW5YHA6sFoXGnHYEFpw130_head
{
this:
np:hasAssertion
dgn-np:NP266714.RAyTIeVhT3SjJP0m--idEYB2sveW5YHA6sFoXGnHYEFpw130_assertion
;
np:hasProvenance
dgn-np:NP266714.RAyTIeVhT3SjJP0m--idEYB2sveW5YHA6sFoXGnHYEFpw130_provenance
;
np:hasPublicationInfo
dgn-np:NP266714.RAyTIeVhT3SjJP0m--idEYB2sveW5YHA6sFoXGnHYEFpw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP266714.RAyTIeVhT3SjJP0m--idEYB2sveW5YHA6sFoXGnHYEFpw130_assertion
a
np:Assertion
.
dgn-np:NP266714.RAyTIeVhT3SjJP0m--idEYB2sveW5YHA6sFoXGnHYEFpw130_provenance
a
np:Provenance
.
dgn-np:NP266714.RAyTIeVhT3SjJP0m--idEYB2sveW5YHA6sFoXGnHYEFpw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP266714.RAyTIeVhT3SjJP0m--idEYB2sveW5YHA6sFoXGnHYEFpw130_assertion
{
miriam-gene:1586
a
ncit:C16612
.
lld:C3277849
a
ncit:C7057
.
dgn-gda:DGNbfc397a8c78bf92f697aafe32be3967a
sio:SIO_000628
miriam-gene:1586
,
lld:C3277849
;
a
sio:SIO_001121
.
}
dgn-np:NP266714.RAyTIeVhT3SjJP0m--idEYB2sveW5YHA6sFoXGnHYEFpw130_provenance
{
dgn-np:NP266714.RAyTIeVhT3SjJP0m--idEYB2sveW5YHA6sFoXGnHYEFpw130_assertion
dcterms:description
"[Isolated 17,20 lyase deficiency is rare, but the identification of its genetic basis and the study of P450c17 enzymology have recently clarified the mechanisms by which DHEA synthesis may be regulated in adrenarche, and have suggested that the lesion underlying polycystic ovary syndrome might involve a serine kinase.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:9890062
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
xsd:date
.
dgn-void:source_evidence_literature
a
eco:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP266714.RAyTIeVhT3SjJP0m--idEYB2sveW5YHA6sFoXGnHYEFpw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:29+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}