@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1016599.RA0O05MYSrRptRJMF2ljdZL9qSvaQ1EC3zfbJ-iNnmRYU
> .
@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:NP1016599.RA0O05MYSrRptRJMF2ljdZL9qSvaQ1EC3zfbJ-iNnmRYU130_head
{
this:
np:hasAssertion
dgn-np:NP1016599.RA0O05MYSrRptRJMF2ljdZL9qSvaQ1EC3zfbJ-iNnmRYU130_assertion
;
np:hasProvenance
dgn-np:NP1016599.RA0O05MYSrRptRJMF2ljdZL9qSvaQ1EC3zfbJ-iNnmRYU130_provenance
;
np:hasPublicationInfo
dgn-np:NP1016599.RA0O05MYSrRptRJMF2ljdZL9qSvaQ1EC3zfbJ-iNnmRYU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1016599.RA0O05MYSrRptRJMF2ljdZL9qSvaQ1EC3zfbJ-iNnmRYU130_assertion
a
np:Assertion
.
dgn-np:NP1016599.RA0O05MYSrRptRJMF2ljdZL9qSvaQ1EC3zfbJ-iNnmRYU130_provenance
a
np:Provenance
.
dgn-np:NP1016599.RA0O05MYSrRptRJMF2ljdZL9qSvaQ1EC3zfbJ-iNnmRYU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1016599.RA0O05MYSrRptRJMF2ljdZL9qSvaQ1EC3zfbJ-iNnmRYU130_assertion
{
miriam-gene:10468
a
ncit:C16612
.
lld:C0029928
a
ncit:C7057
.
dgn-gda:DGNb8965edbff561cb83fa88c956872ccc1
sio:SIO_000628
miriam-gene:10468
,
lld:C0029928
;
a
sio:SIO_001121
.
}
dgn-np:NP1016599.RA0O05MYSrRptRJMF2ljdZL9qSvaQ1EC3zfbJ-iNnmRYU130_provenance
{
dgn-np:NP1016599.RA0O05MYSrRptRJMF2ljdZL9qSvaQ1EC3zfbJ-iNnmRYU130_assertion
dcterms:description
"[The occurrence of the exonic variants of FST gene seems to be dependent on the ethnic background of the subjects under study and its role in the PCOS pathophysiology cannot be established with hitherto available evidence.]. 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-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:NP1016599.RA0O05MYSrRptRJMF2ljdZL9qSvaQ1EC3zfbJ-iNnmRYU130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:49:26+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" .
}