@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP711022.RAOFNfT5C_2KA8yLv604BET5C_GbYQZUsugJZmkWcOc_0> .
@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:NP711022.RAOFNfT5C_2KA8yLv604BET5C_GbYQZUsugJZmkWcOc_0130_head {
  this: np:hasAssertion dgn-np:NP711022.RAOFNfT5C_2KA8yLv604BET5C_GbYQZUsugJZmkWcOc_0130_assertion;
    np:hasProvenance dgn-np:NP711022.RAOFNfT5C_2KA8yLv604BET5C_GbYQZUsugJZmkWcOc_0130_provenance;
    np:hasPublicationInfo dgn-np:NP711022.RAOFNfT5C_2KA8yLv604BET5C_GbYQZUsugJZmkWcOc_0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP711022.RAOFNfT5C_2KA8yLv604BET5C_GbYQZUsugJZmkWcOc_0130_assertion a np:Assertion .
  
  dgn-np:NP711022.RAOFNfT5C_2KA8yLv604BET5C_GbYQZUsugJZmkWcOc_0130_provenance a np:Provenance .
  
  dgn-np:NP711022.RAOFNfT5C_2KA8yLv604BET5C_GbYQZUsugJZmkWcOc_0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP711022.RAOFNfT5C_2KA8yLv604BET5C_GbYQZUsugJZmkWcOc_0130_assertion {
  miriam-gene:1545 a ncit:C16612 .
  
  lld:C0699885 a ncit:C7057 .
  
  dgn-gda:DGN72e784b018cda24b3cb188f04d412fd8 sio:SIO_000628 miriam-gene:1545, lld:C0699885;
    a sio:SIO_001121 .
}

dgn-np:NP711022.RAOFNfT5C_2KA8yLv604BET5C_GbYQZUsugJZmkWcOc_0130_provenance {
  dgn-np:NP711022.RAOFNfT5C_2KA8yLv604BET5C_GbYQZUsugJZmkWcOc_0130_assertion dcterms:description
      "[Our results indicate that inherited absence of GSTT1 gene may be associated with bladder cancer susceptibility, and specific combinations of GSTM1, GSTT1 and CYP1B1 gene polymorphisms may modify bladder cancer risk in the Turkish population, without any association being observed for CYP1A1 gene polymorphism and bladder cancer risk.]. 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:23886208;
    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:NP711022.RAOFNfT5C_2KA8yLv604BET5C_GbYQZUsugJZmkWcOc_0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:12+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" .
}