@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP937034.RA17dwAqIxLpVt2B_2n7TKfqi5yfBovxteJNd8UxIuLb0> .
@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:NP937034.RA17dwAqIxLpVt2B_2n7TKfqi5yfBovxteJNd8UxIuLb0130_head {
  this: np:hasAssertion dgn-np:NP937034.RA17dwAqIxLpVt2B_2n7TKfqi5yfBovxteJNd8UxIuLb0130_assertion;
    np:hasProvenance dgn-np:NP937034.RA17dwAqIxLpVt2B_2n7TKfqi5yfBovxteJNd8UxIuLb0130_provenance;
    np:hasPublicationInfo dgn-np:NP937034.RA17dwAqIxLpVt2B_2n7TKfqi5yfBovxteJNd8UxIuLb0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP937034.RA17dwAqIxLpVt2B_2n7TKfqi5yfBovxteJNd8UxIuLb0130_assertion a np:Assertion .
  
  dgn-np:NP937034.RA17dwAqIxLpVt2B_2n7TKfqi5yfBovxteJNd8UxIuLb0130_provenance a np:Provenance .
  
  dgn-np:NP937034.RA17dwAqIxLpVt2B_2n7TKfqi5yfBovxteJNd8UxIuLb0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP937034.RA17dwAqIxLpVt2B_2n7TKfqi5yfBovxteJNd8UxIuLb0130_assertion {
  miriam-gene:472 a ncit:C16612 .
  
  lld:C0027651 a ncit:C7057 .
  
  dgn-gda:DGN001cbbc6c3572ecb43b138a6d2bf430e sio:SIO_000628 miriam-gene:472, lld:C0027651;
    a sio:SIO_001121 .
}

dgn-np:NP937034.RA17dwAqIxLpVt2B_2n7TKfqi5yfBovxteJNd8UxIuLb0130_provenance {
  dgn-np:NP937034.RA17dwAqIxLpVt2B_2n7TKfqi5yfBovxteJNd8UxIuLb0130_assertion dcterms:description
      "[Furthermore, we propose that the lack of DDR activation avoids the pressure to select for mutations in DDR genes such as p53 or ATM, and the resulting intact DDR machinery may have implications for the exceptional curability of TGCTs by DNA damaging therapies.]. 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:17573848;
    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:NP937034.RA17dwAqIxLpVt2B_2n7TKfqi5yfBovxteJNd8UxIuLb0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:34+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" .
}