@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1331168.RAFetU-WDIlE6qO9PFVTLFrAlX_cE6YPdSiVXX_HL2OSY
> .
@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:NP1331168.RAFetU-WDIlE6qO9PFVTLFrAlX_cE6YPdSiVXX_HL2OSY130_head
{
this:
np:hasAssertion
dgn-np:NP1331168.RAFetU-WDIlE6qO9PFVTLFrAlX_cE6YPdSiVXX_HL2OSY130_assertion
;
np:hasProvenance
dgn-np:NP1331168.RAFetU-WDIlE6qO9PFVTLFrAlX_cE6YPdSiVXX_HL2OSY130_provenance
;
np:hasPublicationInfo
dgn-np:NP1331168.RAFetU-WDIlE6qO9PFVTLFrAlX_cE6YPdSiVXX_HL2OSY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1331168.RAFetU-WDIlE6qO9PFVTLFrAlX_cE6YPdSiVXX_HL2OSY130_assertion
a
np:Assertion
.
dgn-np:NP1331168.RAFetU-WDIlE6qO9PFVTLFrAlX_cE6YPdSiVXX_HL2OSY130_provenance
a
np:Provenance
.
dgn-np:NP1331168.RAFetU-WDIlE6qO9PFVTLFrAlX_cE6YPdSiVXX_HL2OSY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1331168.RAFetU-WDIlE6qO9PFVTLFrAlX_cE6YPdSiVXX_HL2OSY130_assertion
{
miriam-gene:3630
a
ncit:C16612
.
lld:C0020459
a
ncit:C7057
.
dgn-gda:DGN2234819b100af711f10505c660df7ff1
sio:SIO_000628
miriam-gene:3630
,
lld:C0020459
;
a
sio:SIO_001121
.
}
dgn-np:NP1331168.RAFetU-WDIlE6qO9PFVTLFrAlX_cE6YPdSiVXX_HL2OSY130_provenance
{
dgn-np:NP1331168.RAFetU-WDIlE6qO9PFVTLFrAlX_cE6YPdSiVXX_HL2OSY130_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-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:NP1331168.RAFetU-WDIlE6qO9PFVTLFrAlX_cE6YPdSiVXX_HL2OSY130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:49+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" .
}