@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1294183.RAM83RvhJWxLrZvbq7ANdK6ts12emELi7SOmDwdkW72_g> .
@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:NP1294183.RAM83RvhJWxLrZvbq7ANdK6ts12emELi7SOmDwdkW72_g130_head {
  this: np:hasAssertion dgn-np:NP1294183.RAM83RvhJWxLrZvbq7ANdK6ts12emELi7SOmDwdkW72_g130_assertion;
    np:hasProvenance dgn-np:NP1294183.RAM83RvhJWxLrZvbq7ANdK6ts12emELi7SOmDwdkW72_g130_provenance;
    np:hasPublicationInfo dgn-np:NP1294183.RAM83RvhJWxLrZvbq7ANdK6ts12emELi7SOmDwdkW72_g130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1294183.RAM83RvhJWxLrZvbq7ANdK6ts12emELi7SOmDwdkW72_g130_assertion a np:Assertion .
  
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  dgn-np:NP1294183.RAM83RvhJWxLrZvbq7ANdK6ts12emELi7SOmDwdkW72_g130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1294183.RAM83RvhJWxLrZvbq7ANdK6ts12emELi7SOmDwdkW72_g130_assertion {
  miriam-gene:54658 a ncit:C16612 .
  
  lld:C0005684 a ncit:C7057 .
  
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dgn-np:NP1294183.RAM83RvhJWxLrZvbq7ANdK6ts12emELi7SOmDwdkW72_g130_provenance {
  dgn-np:NP1294183.RAM83RvhJWxLrZvbq7ANdK6ts12emELi7SOmDwdkW72_g130_assertion dcterms:description
      "[Using data on high-risk occupations for 2258 case patients and 2410 control patients from two bladder cancer studies, we observed that three of 16 known or candidate bladder cancer susceptibility variants displayed statistically significant and consistent evidence of additive interactions; specifically, the GSTM1 deletion polymorphism (P interaction ≤ .001), rs11892031 (UGT1A, P interaction = .01), and rs798766 (TMEM129-TACC3-FGFR3, P interaction = .03).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
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  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^xsd:date .
  
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    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en;
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dgn-np:NP1294183.RAM83RvhJWxLrZvbq7ANdK6ts12emELi7SOmDwdkW72_g130_publicationInfo {
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    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
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