@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP636747.RAKPSg6iyg6uFWVhhIG2D1vJli17GSryzoFDhl6RIr7rk
> .
@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:NP636747.RAKPSg6iyg6uFWVhhIG2D1vJli17GSryzoFDhl6RIr7rk130_head
{
this:
np:hasAssertion
dgn-np:NP636747.RAKPSg6iyg6uFWVhhIG2D1vJli17GSryzoFDhl6RIr7rk130_assertion
;
np:hasProvenance
dgn-np:NP636747.RAKPSg6iyg6uFWVhhIG2D1vJli17GSryzoFDhl6RIr7rk130_provenance
;
np:hasPublicationInfo
dgn-np:NP636747.RAKPSg6iyg6uFWVhhIG2D1vJli17GSryzoFDhl6RIr7rk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP636747.RAKPSg6iyg6uFWVhhIG2D1vJli17GSryzoFDhl6RIr7rk130_assertion
a
np:Assertion
.
dgn-np:NP636747.RAKPSg6iyg6uFWVhhIG2D1vJli17GSryzoFDhl6RIr7rk130_provenance
a
np:Provenance
.
dgn-np:NP636747.RAKPSg6iyg6uFWVhhIG2D1vJli17GSryzoFDhl6RIr7rk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP636747.RAKPSg6iyg6uFWVhhIG2D1vJli17GSryzoFDhl6RIr7rk130_assertion
{
miriam-gene:3643
a
ncit:C16612
.
lld:C0206081
a
ncit:C7057
.
dgn-gda:DGN328806f15d009223c63178de1e7e8b60
sio:SIO_000628
miriam-gene:3643
,
lld:C0206081
;
a
sio:SIO_001121
.
}
dgn-np:NP636747.RAKPSg6iyg6uFWVhhIG2D1vJli17GSryzoFDhl6RIr7rk130_provenance
{
dgn-np:NP636747.RAKPSg6iyg6uFWVhhIG2D1vJli17GSryzoFDhl6RIr7rk130_assertion
dcterms:description
"[This evidence includes: (1) mutations in the insulin receptor gene that cause severe hyperinsulinemia appear to be associated with ovarian hyperandrogenism, (2) insulin stimulates ovarian thecal and stromal androgen secretion in vitro, and (3) in some experimental models, manipulation of circulating insulin concentrations results in changes in circulating androgens.]. 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:8064699
;
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:NP636747.RAKPSg6iyg6uFWVhhIG2D1vJli17GSryzoFDhl6RIr7rk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:24+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" .
}