@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP452207.RAb6HWbaUT0Ipn_NjUBJmAJinO1JXxpoVpNdiH8Y-xLnk
> .
@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:NP452207.RAb6HWbaUT0Ipn_NjUBJmAJinO1JXxpoVpNdiH8Y-xLnk130_head
{
this:
np:hasAssertion
dgn-np:NP452207.RAb6HWbaUT0Ipn_NjUBJmAJinO1JXxpoVpNdiH8Y-xLnk130_assertion
;
np:hasProvenance
dgn-np:NP452207.RAb6HWbaUT0Ipn_NjUBJmAJinO1JXxpoVpNdiH8Y-xLnk130_provenance
;
np:hasPublicationInfo
dgn-np:NP452207.RAb6HWbaUT0Ipn_NjUBJmAJinO1JXxpoVpNdiH8Y-xLnk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP452207.RAb6HWbaUT0Ipn_NjUBJmAJinO1JXxpoVpNdiH8Y-xLnk130_assertion
a
np:Assertion
.
dgn-np:NP452207.RAb6HWbaUT0Ipn_NjUBJmAJinO1JXxpoVpNdiH8Y-xLnk130_provenance
a
np:Provenance
.
dgn-np:NP452207.RAb6HWbaUT0Ipn_NjUBJmAJinO1JXxpoVpNdiH8Y-xLnk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP452207.RAb6HWbaUT0Ipn_NjUBJmAJinO1JXxpoVpNdiH8Y-xLnk130_assertion
{
miriam-gene:6715
a
ncit:C16612
.
lld:C0032460
a
ncit:C7057
.
dgn-gda:DGN8e8f25e6fd5583b9da8e3abee3bf0a9b
sio:SIO_000628
miriam-gene:6715
,
lld:C0032460
;
a
sio:SIO_001121
.
}
dgn-np:NP452207.RAb6HWbaUT0Ipn_NjUBJmAJinO1JXxpoVpNdiH8Y-xLnk130_provenance
{
dgn-np:NP452207.RAb6HWbaUT0Ipn_NjUBJmAJinO1JXxpoVpNdiH8Y-xLnk130_assertion
dcterms:description
"[The objective of the study was to test the hypothesis that haplotypes in the SRD5A1 and SRD5A2 genes are risk factors for PCOS and the severity of hirsutism in affected women.]. 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:16849416
;
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:NP452207.RAb6HWbaUT0Ipn_NjUBJmAJinO1JXxpoVpNdiH8Y-xLnk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:29+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" .
}