@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP834078.RA1HBNtcRsNf0L6kKNwEEx51nMD4pR_JtCHrPXamEx77Y> .
@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:NP834078.RA1HBNtcRsNf0L6kKNwEEx51nMD4pR_JtCHrPXamEx77Y130_head {
  this: np:hasAssertion dgn-np:NP834078.RA1HBNtcRsNf0L6kKNwEEx51nMD4pR_JtCHrPXamEx77Y130_assertion;
    np:hasProvenance dgn-np:NP834078.RA1HBNtcRsNf0L6kKNwEEx51nMD4pR_JtCHrPXamEx77Y130_provenance;
    np:hasPublicationInfo dgn-np:NP834078.RA1HBNtcRsNf0L6kKNwEEx51nMD4pR_JtCHrPXamEx77Y130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP834078.RA1HBNtcRsNf0L6kKNwEEx51nMD4pR_JtCHrPXamEx77Y130_assertion a np:Assertion .
  
  dgn-np:NP834078.RA1HBNtcRsNf0L6kKNwEEx51nMD4pR_JtCHrPXamEx77Y130_provenance a np:Provenance .
  
  dgn-np:NP834078.RA1HBNtcRsNf0L6kKNwEEx51nMD4pR_JtCHrPXamEx77Y130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP834078.RA1HBNtcRsNf0L6kKNwEEx51nMD4pR_JtCHrPXamEx77Y130_assertion {
  miriam-gene:7157 a ncit:C16612 .
  
  lld:C1882062 a ncit:C7057 .
  
  dgn-gda:DGNb096e75ca628fa12964409a3b70f757c sio:SIO_000628 miriam-gene:7157, lld:C1882062;
    a sio:SIO_001121 .
}

dgn-np:NP834078.RA1HBNtcRsNf0L6kKNwEEx51nMD4pR_JtCHrPXamEx77Y130_provenance {
  dgn-np:NP834078.RA1HBNtcRsNf0L6kKNwEEx51nMD4pR_JtCHrPXamEx77Y130_assertion dcterms:description
      "[To determine whether this p53 genotype influences individual risk of urologic cancer and/or its progression, we used polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) analysis to assay the allelic frequencies of this polymorphism in 85 renal cell carcinoma patients, 151 urothelial cancer patients, 33 testicular cancer patients, 28 prostatic cancer patients and 56 patients without neoplastic disease.]. 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:7559095;
    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:NP834078.RA1HBNtcRsNf0L6kKNwEEx51nMD4pR_JtCHrPXamEx77Y130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:30+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" .
}