@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP505084.RAde21FOLWMSBP8eC4PwxNj2sO0AuPvA7-q36so39omaI> .
@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:NP505084.RAde21FOLWMSBP8eC4PwxNj2sO0AuPvA7-q36so39omaI130_head {
  this: np:hasAssertion dgn-np:NP505084.RAde21FOLWMSBP8eC4PwxNj2sO0AuPvA7-q36so39omaI130_assertion;
    np:hasProvenance dgn-np:NP505084.RAde21FOLWMSBP8eC4PwxNj2sO0AuPvA7-q36so39omaI130_provenance;
    np:hasPublicationInfo dgn-np:NP505084.RAde21FOLWMSBP8eC4PwxNj2sO0AuPvA7-q36so39omaI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP505084.RAde21FOLWMSBP8eC4PwxNj2sO0AuPvA7-q36so39omaI130_assertion a np:Assertion .
  
  dgn-np:NP505084.RAde21FOLWMSBP8eC4PwxNj2sO0AuPvA7-q36so39omaI130_provenance a np:Provenance .
  
  dgn-np:NP505084.RAde21FOLWMSBP8eC4PwxNj2sO0AuPvA7-q36so39omaI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP505084.RAde21FOLWMSBP8eC4PwxNj2sO0AuPvA7-q36so39omaI130_assertion {
  miriam-gene:675 a ncit:C16612 .
  
  lld:C0021359 a ncit:C7057 .
  
  dgn-gda:DGN447a32f46d4c40ea54f32c0b05f2640c sio:SIO_000628 miriam-gene:675, lld:C0021359;
    a sio:SIO_001121 .
}

dgn-np:NP505084.RAde21FOLWMSBP8eC4PwxNj2sO0AuPvA7-q36so39omaI130_provenance {
  dgn-np:NP505084.RAde21FOLWMSBP8eC4PwxNj2sO0AuPvA7-q36so39omaI130_assertion dcterms:description
      "[This preliminary finding does not support the assumption that the presence of BRCA1 and BRCA2 mutations in some infertility patients treated by fertility drugs could explain the subsequent development of epithelial ovarian cancer in these 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:10609497;
    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:NP505084.RAde21FOLWMSBP8eC4PwxNj2sO0AuPvA7-q36so39omaI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:01+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" .
}