@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1413668.RArj8VL2lPTdcPynHt8vsny7fEk9K6BLoEscpeb4TtiIY
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP1413668.RArj8VL2lPTdcPynHt8vsny7fEk9K6BLoEscpeb4TtiIY130_head
{
this:
np:hasAssertion
dgn-np:NP1413668.RArj8VL2lPTdcPynHt8vsny7fEk9K6BLoEscpeb4TtiIY130_assertion
;
np:hasProvenance
dgn-np:NP1413668.RArj8VL2lPTdcPynHt8vsny7fEk9K6BLoEscpeb4TtiIY130_provenance
;
np:hasPublicationInfo
dgn-np:NP1413668.RArj8VL2lPTdcPynHt8vsny7fEk9K6BLoEscpeb4TtiIY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1413668.RArj8VL2lPTdcPynHt8vsny7fEk9K6BLoEscpeb4TtiIY130_assertion
a
np:Assertion
.
dgn-np:NP1413668.RArj8VL2lPTdcPynHt8vsny7fEk9K6BLoEscpeb4TtiIY130_provenance
a
np:Provenance
.
dgn-np:NP1413668.RArj8VL2lPTdcPynHt8vsny7fEk9K6BLoEscpeb4TtiIY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1413668.RArj8VL2lPTdcPynHt8vsny7fEk9K6BLoEscpeb4TtiIY130_assertion
{
miriam-gene:1583
a
ncit:C16612
.
lld:C0032460
a
ncit:C7057
.
dgn-gda:DGNd0d4b7abcf93fedcb3700b63d43227f0
sio:SIO_000628
miriam-gene:1583
,
lld:C0032460
;
a
sio:SIO_001121
.
}
dgn-np:NP1413668.RArj8VL2lPTdcPynHt8vsny7fEk9K6BLoEscpeb4TtiIY130_provenance
{
dgn-np:NP1413668.RArj8VL2lPTdcPynHt8vsny7fEk9K6BLoEscpeb4TtiIY130_assertion
dcterms:description
"[Differences in expression of CYP11a could account for variation in androgen production in women who have polycystic ovaries and those subjects who are homozygous for III alleles at the insulin gene VNTR locus are more likely to be hyperinsulinaemic.]. 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:9922108
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1413668.RArj8VL2lPTdcPynHt8vsny7fEk9K6BLoEscpeb4TtiIY130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:52:27+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}