@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP792571.RADGZd4Z2qO0MYgU2aaMxZ47kdldir57NISEsIawVPEnk> .
@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:NP792571.RADGZd4Z2qO0MYgU2aaMxZ47kdldir57NISEsIawVPEnk130_head {
  this: np:hasAssertion dgn-np:NP792571.RADGZd4Z2qO0MYgU2aaMxZ47kdldir57NISEsIawVPEnk130_assertion;
    np:hasProvenance dgn-np:NP792571.RADGZd4Z2qO0MYgU2aaMxZ47kdldir57NISEsIawVPEnk130_provenance;
    np:hasPublicationInfo dgn-np:NP792571.RADGZd4Z2qO0MYgU2aaMxZ47kdldir57NISEsIawVPEnk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP792571.RADGZd4Z2qO0MYgU2aaMxZ47kdldir57NISEsIawVPEnk130_assertion a np:Assertion .
  
  dgn-np:NP792571.RADGZd4Z2qO0MYgU2aaMxZ47kdldir57NISEsIawVPEnk130_provenance a np:Provenance .
  
  dgn-np:NP792571.RADGZd4Z2qO0MYgU2aaMxZ47kdldir57NISEsIawVPEnk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP792571.RADGZd4Z2qO0MYgU2aaMxZ47kdldir57NISEsIawVPEnk130_assertion {
  miriam-gene:5728 a ncit:C16612 .
  
  lld:C0206681 a ncit:C7057 .
  
  dgn-gda:DGN4a5b59e572b131763a71fbbea8508611 sio:SIO_000628 miriam-gene:5728, lld:C0206681;
    a sio:SIO_001121 .
}

dgn-np:NP792571.RADGZd4Z2qO0MYgU2aaMxZ47kdldir57NISEsIawVPEnk130_provenance {
  dgn-np:NP792571.RADGZd4Z2qO0MYgU2aaMxZ47kdldir57NISEsIawVPEnk130_assertion dcterms:description
      "[In addition, two cases of mixed serous and clear cell carcinoma showed an identical mutation of the p53 gene in the histologically distinct components and one case of mixed clear cell and endometrioid carcinoma had identical mutations in the PTEN and p53 genes, and microsatellite instability in both components.]. 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:14976538;
    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:NP792571.RADGZd4Z2qO0MYgU2aaMxZ47kdldir57NISEsIawVPEnk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:06+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" .
}