@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP195115.RATCGMHFRkA6YtWmXFIKAOWxtnY5b2rQ86BotreHIACUM
> .
@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:NP195115.RATCGMHFRkA6YtWmXFIKAOWxtnY5b2rQ86BotreHIACUM130_head
{
this:
np:hasAssertion
dgn-np:NP195115.RATCGMHFRkA6YtWmXFIKAOWxtnY5b2rQ86BotreHIACUM130_assertion
;
np:hasProvenance
dgn-np:NP195115.RATCGMHFRkA6YtWmXFIKAOWxtnY5b2rQ86BotreHIACUM130_provenance
;
np:hasPublicationInfo
dgn-np:NP195115.RATCGMHFRkA6YtWmXFIKAOWxtnY5b2rQ86BotreHIACUM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP195115.RATCGMHFRkA6YtWmXFIKAOWxtnY5b2rQ86BotreHIACUM130_assertion
a
np:Assertion
.
dgn-np:NP195115.RATCGMHFRkA6YtWmXFIKAOWxtnY5b2rQ86BotreHIACUM130_provenance
a
np:Provenance
.
dgn-np:NP195115.RATCGMHFRkA6YtWmXFIKAOWxtnY5b2rQ86BotreHIACUM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP195115.RATCGMHFRkA6YtWmXFIKAOWxtnY5b2rQ86BotreHIACUM130_assertion
{
miriam-gene:10468
a
ncit:C16612
.
lld:C0032460
a
ncit:C7057
.
dgn-gda:DGN81fc327dd30bff396b80c91ae5660bac
sio:SIO_000628
miriam-gene:10468
,
lld:C0032460
;
a
sio:SIO_001121
.
}
dgn-np:NP195115.RATCGMHFRkA6YtWmXFIKAOWxtnY5b2rQ86BotreHIACUM130_provenance
{
dgn-np:NP195115.RATCGMHFRkA6YtWmXFIKAOWxtnY5b2rQ86BotreHIACUM130_assertion
dcterms:description
"[Subsequently, a couple of studies outside India investigated the FST gene for the presence of any mutations and its association with PCOS and the results were found to be largely inconsistent probably due to differences in the ethnic backgrounds and small sample sizes.]. 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:23023351
;
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:NP195115.RATCGMHFRkA6YtWmXFIKAOWxtnY5b2rQ86BotreHIACUM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:47+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" .
}