@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP487646.RAAoNZj4n2_dqKnZ_FmiBKCFVypN5BSh1__g4LJzJe35Q> .
@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:NP487646.RAAoNZj4n2_dqKnZ_FmiBKCFVypN5BSh1__g4LJzJe35Q130_head {
  this: np:hasAssertion dgn-np:NP487646.RAAoNZj4n2_dqKnZ_FmiBKCFVypN5BSh1__g4LJzJe35Q130_assertion;
    np:hasProvenance dgn-np:NP487646.RAAoNZj4n2_dqKnZ_FmiBKCFVypN5BSh1__g4LJzJe35Q130_provenance;
    np:hasPublicationInfo dgn-np:NP487646.RAAoNZj4n2_dqKnZ_FmiBKCFVypN5BSh1__g4LJzJe35Q130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP487646.RAAoNZj4n2_dqKnZ_FmiBKCFVypN5BSh1__g4LJzJe35Q130_assertion a np:Assertion .
  
  dgn-np:NP487646.RAAoNZj4n2_dqKnZ_FmiBKCFVypN5BSh1__g4LJzJe35Q130_provenance a np:Provenance .
  
  dgn-np:NP487646.RAAoNZj4n2_dqKnZ_FmiBKCFVypN5BSh1__g4LJzJe35Q130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP487646.RAAoNZj4n2_dqKnZ_FmiBKCFVypN5BSh1__g4LJzJe35Q130_assertion {
  miriam-gene:5728 a ncit:C16612 .
  
  lld:C0007103 a ncit:C7057 .
  
  dgn-gda:DGN662603816c0b28693e934bebf52c614f sio:SIO_000628 miriam-gene:5728, lld:C0007103;
    a sio:SIO_001121 .
}

dgn-np:NP487646.RAAoNZj4n2_dqKnZ_FmiBKCFVypN5BSh1__g4LJzJe35Q130_provenance {
  dgn-np:NP487646.RAAoNZj4n2_dqKnZ_FmiBKCFVypN5BSh1__g4LJzJe35Q130_assertion dcterms:description
      "[Although these data do not preclude the possibility of an increased risk of endometrial cancer in association with the Cowden syndrome, they indicate that germline PTEN mutations do not account for a significant proportion of genetic attributable risk for endometrial carcinoma.]. 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:15589575;
    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:NP487646.RAAoNZj4n2_dqKnZ_FmiBKCFVypN5BSh1__g4LJzJe35Q130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:51+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" .
}