@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" .
}