@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP145793.RAmcmFaLdUDXMHf18SiURE31yeeJ2mFOG752pIT-ibmOc> .
@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:NP145793.RAmcmFaLdUDXMHf18SiURE31yeeJ2mFOG752pIT-ibmOc130_head {
  this: np:hasAssertion dgn-np:NP145793.RAmcmFaLdUDXMHf18SiURE31yeeJ2mFOG752pIT-ibmOc130_assertion;
    np:hasProvenance dgn-np:NP145793.RAmcmFaLdUDXMHf18SiURE31yeeJ2mFOG752pIT-ibmOc130_provenance;
    np:hasPublicationInfo dgn-np:NP145793.RAmcmFaLdUDXMHf18SiURE31yeeJ2mFOG752pIT-ibmOc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP145793.RAmcmFaLdUDXMHf18SiURE31yeeJ2mFOG752pIT-ibmOc130_assertion a np:Assertion .
  
  dgn-np:NP145793.RAmcmFaLdUDXMHf18SiURE31yeeJ2mFOG752pIT-ibmOc130_provenance a np:Provenance .
  
  dgn-np:NP145793.RAmcmFaLdUDXMHf18SiURE31yeeJ2mFOG752pIT-ibmOc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP145793.RAmcmFaLdUDXMHf18SiURE31yeeJ2mFOG752pIT-ibmOc130_assertion {
  miriam-gene:1543 a ncit:C16612 .
  
  lld:C0016978 a ncit:C7057 .
  
  dgn-gda:DGNb713190c7e9b1e3e4ba458d47662c050 sio:SIO_000628 miriam-gene:1543, lld:C0016978;
    a sio:SIO_001122 .
}

dgn-np:NP145793.RAmcmFaLdUDXMHf18SiURE31yeeJ2mFOG752pIT-ibmOc130_provenance {
  dgn-np:NP145793.RAmcmFaLdUDXMHf18SiURE31yeeJ2mFOG752pIT-ibmOc130_assertion dcterms:description
      "[These results suggest that the Val allele of CYP1A1 Ile462Val polymorphism and the Pro allele of TP53 Arg72Pro polymorphism contribute to an increased risk of gallbladder cancer among Japanese women and men, respectively.]. 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:17531965;
    prov:wasDerivedFrom dgn-void:lhgdn-20090331;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:lhgdn-20090331 pav:importedOn "2009-03-31"^^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:NP145793.RAmcmFaLdUDXMHf18SiURE31yeeJ2mFOG752pIT-ibmOc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:16+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" .
}