@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP429083.RAZH_MytIHNRWNAcI7jaMN3noQmli9zYcOQFpqgmb_A78> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .
dgn-np:NP429083.RAZH_MytIHNRWNAcI7jaMN3noQmli9zYcOQFpqgmb_A78130_head {
  this: np:hasAssertion dgn-np:NP429083.RAZH_MytIHNRWNAcI7jaMN3noQmli9zYcOQFpqgmb_A78130_assertion ;
    np:hasProvenance dgn-np:NP429083.RAZH_MytIHNRWNAcI7jaMN3noQmli9zYcOQFpqgmb_A78130_provenance ;
    np:hasPublicationInfo dgn-np:NP429083.RAZH_MytIHNRWNAcI7jaMN3noQmli9zYcOQFpqgmb_A78130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP429083.RAZH_MytIHNRWNAcI7jaMN3noQmli9zYcOQFpqgmb_A78130_assertion a np:Assertion .
  dgn-np:NP429083.RAZH_MytIHNRWNAcI7jaMN3noQmli9zYcOQFpqgmb_A78130_provenance a np:Provenance .
  dgn-np:NP429083.RAZH_MytIHNRWNAcI7jaMN3noQmli9zYcOQFpqgmb_A78130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP429083.RAZH_MytIHNRWNAcI7jaMN3noQmli9zYcOQFpqgmb_A78130_assertion {
  miriam-gene:7157 a ncit:C16612 .
  lld:C0178874 a ncit:C7057 .
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}
dgn-np:NP429083.RAZH_MytIHNRWNAcI7jaMN3noQmli9zYcOQFpqgmb_A78130_provenance {
  dgn-np:NP429083.RAZH_MytIHNRWNAcI7jaMN3noQmli9zYcOQFpqgmb_A78130_assertion dcterms:description "[Mutation and deletion of the p53 tumor suppressor gene are arguably the most prevalent among the multiple genetic alterations found in human bladder cancer, but these p53 defects are primarily associated with the advanced diseases, and their roles in bladder tumor initiation and in synergizing with oncogenes in tumor progression have yet to be defined.]. 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:14737103 ;
    prov:wasDerivedFrom dgn-void:befree-2016 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP429083.RAZH_MytIHNRWNAcI7jaMN3noQmli9zYcOQFpqgmb_A78130_publicationInfo {
  this: dcterms:created "2016-05-13T12:44:59+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159> ;
    pav:version "v4.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}