@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP787651.RAhTeJ-GqHYsmhZsumc8ajC4kDdo5tG1HoJW4LQXQQDTg> .
@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:NP787651.RAhTeJ-GqHYsmhZsumc8ajC4kDdo5tG1HoJW4LQXQQDTg130_head {
  this: np:hasAssertion dgn-np:NP787651.RAhTeJ-GqHYsmhZsumc8ajC4kDdo5tG1HoJW4LQXQQDTg130_assertion;
    np:hasProvenance dgn-np:NP787651.RAhTeJ-GqHYsmhZsumc8ajC4kDdo5tG1HoJW4LQXQQDTg130_provenance;
    np:hasPublicationInfo dgn-np:NP787651.RAhTeJ-GqHYsmhZsumc8ajC4kDdo5tG1HoJW4LQXQQDTg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP787651.RAhTeJ-GqHYsmhZsumc8ajC4kDdo5tG1HoJW4LQXQQDTg130_assertion a np:Assertion .
  
  dgn-np:NP787651.RAhTeJ-GqHYsmhZsumc8ajC4kDdo5tG1HoJW4LQXQQDTg130_provenance a np:Provenance .
  
  dgn-np:NP787651.RAhTeJ-GqHYsmhZsumc8ajC4kDdo5tG1HoJW4LQXQQDTg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP787651.RAhTeJ-GqHYsmhZsumc8ajC4kDdo5tG1HoJW4LQXQQDTg130_assertion {
  miriam-gene:8289 a ncit:C16612 .
  
  lld:C0014175 a ncit:C7057 .
  
  dgn-gda:DGNa9c166c4657c2e101d00fad7a462cdfb sio:SIO_000628 miriam-gene:8289, lld:C0014175;
    a sio:SIO_001121 .
}

dgn-np:NP787651.RAhTeJ-GqHYsmhZsumc8ajC4kDdo5tG1HoJW4LQXQQDTg130_provenance {
  dgn-np:NP787651.RAhTeJ-GqHYsmhZsumc8ajC4kDdo5tG1HoJW4LQXQQDTg130_assertion dcterms:description
      "[In the last few years, mutations in ARID1A and PIK3CA have been described in a substantial fraction of cases of ovarian clear cell carcinoma, yet the paper by Yamamoto et al in this issue of The Journal of Pathology reveals that PIK3CA mutations can be detected in precursor endometriosis tissues.]. 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:21898874;
    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:NP787651.RAhTeJ-GqHYsmhZsumc8ajC4kDdo5tG1HoJW4LQXQQDTg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:00+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" .
}