@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP614773.RAV6dl8THs3aY8M_qHGQ0Icmtgmh-OGI16CTborQLHP1Q> .
@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:NP614773.RAV6dl8THs3aY8M_qHGQ0Icmtgmh-OGI16CTborQLHP1Q130_head {
  this: np:hasAssertion dgn-np:NP614773.RAV6dl8THs3aY8M_qHGQ0Icmtgmh-OGI16CTborQLHP1Q130_assertion;
    np:hasProvenance dgn-np:NP614773.RAV6dl8THs3aY8M_qHGQ0Icmtgmh-OGI16CTborQLHP1Q130_provenance;
    np:hasPublicationInfo dgn-np:NP614773.RAV6dl8THs3aY8M_qHGQ0Icmtgmh-OGI16CTborQLHP1Q130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP614773.RAV6dl8THs3aY8M_qHGQ0Icmtgmh-OGI16CTborQLHP1Q130_assertion a np:Assertion .
  
  dgn-np:NP614773.RAV6dl8THs3aY8M_qHGQ0Icmtgmh-OGI16CTborQLHP1Q130_provenance a np:Provenance .
  
  dgn-np:NP614773.RAV6dl8THs3aY8M_qHGQ0Icmtgmh-OGI16CTborQLHP1Q130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP614773.RAV6dl8THs3aY8M_qHGQ0Icmtgmh-OGI16CTborQLHP1Q130_assertion {
  miriam-gene:8289 a ncit:C16612 .
  
  lld:C0014175 a ncit:C7057 .
  
  dgn-gda:DGNe727f069ac0faf78a9c5303fb09879ec sio:SIO_000628 miriam-gene:8289, lld:C0014175;
    a sio:SIO_001121 .
}

dgn-np:NP614773.RAV6dl8THs3aY8M_qHGQ0Icmtgmh-OGI16CTborQLHP1Q130_provenance {
  dgn-np:NP614773.RAV6dl8THs3aY8M_qHGQ0Icmtgmh-OGI16CTborQLHP1Q130_assertion dcterms:description
      "[Endometriosis is characterized by genetic instability: like neoplasms endometriosis seems to be monoclonal in origin, several studies have documented loss of heterozygosity (LOH) in endometriosis, data suggest that mutation of the tumor suppressor gene PTEN play a part in the malignant transformation of endometriosis, some studies have revealed TP53 mutations in endometriotic lesions, and mutation of ARID1A seems to be an important early event in the malignant transformation of endometriosis to endometrioid and clear cell carcinomas.]. 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:22032835;
    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:NP614773.RAV6dl8THs3aY8M_qHGQ0Icmtgmh-OGI16CTborQLHP1Q130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:11+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" .
}