@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP164945.RAJywfARh37393X3Rg2MGQvFWPW6gsQ58dFJkYG5s50Kk> .
@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:NP164945.RAJywfARh37393X3Rg2MGQvFWPW6gsQ58dFJkYG5s50Kk130_head {
  this: np:hasAssertion dgn-np:NP164945.RAJywfARh37393X3Rg2MGQvFWPW6gsQ58dFJkYG5s50Kk130_assertion;
    np:hasProvenance dgn-np:NP164945.RAJywfARh37393X3Rg2MGQvFWPW6gsQ58dFJkYG5s50Kk130_provenance;
    np:hasPublicationInfo dgn-np:NP164945.RAJywfARh37393X3Rg2MGQvFWPW6gsQ58dFJkYG5s50Kk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP164945.RAJywfARh37393X3Rg2MGQvFWPW6gsQ58dFJkYG5s50Kk130_assertion a np:Assertion .
  
  dgn-np:NP164945.RAJywfARh37393X3Rg2MGQvFWPW6gsQ58dFJkYG5s50Kk130_provenance a np:Provenance .
  
  dgn-np:NP164945.RAJywfARh37393X3Rg2MGQvFWPW6gsQ58dFJkYG5s50Kk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP164945.RAJywfARh37393X3Rg2MGQvFWPW6gsQ58dFJkYG5s50Kk130_assertion {
  miriam-gene:7157 a ncit:C16612 .
  
  lld:C0220641 a ncit:C7057 .
  
  dgn-gda:DGNd12199cdcdd9047ff9056f060b4d7689 sio:SIO_000628 miriam-gene:7157, lld:C0220641;
    a sio:SIO_001121 .
}

dgn-np:NP164945.RAJywfARh37393X3Rg2MGQvFWPW6gsQ58dFJkYG5s50Kk130_provenance {
  dgn-np:NP164945.RAJywfARh37393X3Rg2MGQvFWPW6gsQ58dFJkYG5s50Kk130_assertion dcterms:description
      "[There was a significant association between the prevalence of p53 mutations in oral tumors and CYP1A1 genotyping patterns in these oral cancer patients, with the highest p53 mutation prevalence observed in subjects with the CYP1A1 [val]/GSTM1 [+] genotype (OR = 6.0; CI = 1.2-29.7).]. 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:9525287;
    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:NP164945.RAJywfARh37393X3Rg2MGQvFWPW6gsQ58dFJkYG5s50Kk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:29+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" .
}