@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP389524.RACk0dUG9hOJ01Pn7pUnCD7RHX_zOyuCF10-qrkiHajTc> .
@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:NP389524.RACk0dUG9hOJ01Pn7pUnCD7RHX_zOyuCF10-qrkiHajTc130_head {
  this: np:hasAssertion dgn-np:NP389524.RACk0dUG9hOJ01Pn7pUnCD7RHX_zOyuCF10-qrkiHajTc130_assertion;
    np:hasProvenance dgn-np:NP389524.RACk0dUG9hOJ01Pn7pUnCD7RHX_zOyuCF10-qrkiHajTc130_provenance;
    np:hasPublicationInfo dgn-np:NP389524.RACk0dUG9hOJ01Pn7pUnCD7RHX_zOyuCF10-qrkiHajTc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP389524.RACk0dUG9hOJ01Pn7pUnCD7RHX_zOyuCF10-qrkiHajTc130_assertion a np:Assertion .
  
  dgn-np:NP389524.RACk0dUG9hOJ01Pn7pUnCD7RHX_zOyuCF10-qrkiHajTc130_provenance a np:Provenance .
  
  dgn-np:NP389524.RACk0dUG9hOJ01Pn7pUnCD7RHX_zOyuCF10-qrkiHajTc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP389524.RACk0dUG9hOJ01Pn7pUnCD7RHX_zOyuCF10-qrkiHajTc130_assertion {
  miriam-gene:1869 a ncit:C16612 .
  
  lld:C0006826 a ncit:C7057 .
  
  dgn-gda:DGN096ae7f9fdc41c3485715c966e30d34a sio:SIO_000628 miriam-gene:1869, lld:C0006826;
    a sio:SIO_001121 .
}

dgn-np:NP389524.RACk0dUG9hOJ01Pn7pUnCD7RHX_zOyuCF10-qrkiHajTc130_provenance {
  dgn-np:NP389524.RACk0dUG9hOJ01Pn7pUnCD7RHX_zOyuCF10-qrkiHajTc130_assertion dcterms:description
      "[Possible reasons for E2F1 mediated aggressiveness are defects in cell death pathways caused by epigenetic inactivation of important tumor suppressor genes, which often occur in late stage cancer and contribute to chemoresistance.]. 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:23377972;
    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:NP389524.RACk0dUG9hOJ01Pn7pUnCD7RHX_zOyuCF10-qrkiHajTc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:52+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" .
}