@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP46140.RAd2vslhcjVvSWjeWmE_GgXpPfNoXylSvKKyoKnu5In6Y> .
@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:NP46140.RAd2vslhcjVvSWjeWmE_GgXpPfNoXylSvKKyoKnu5In6Y130_head {
  this: np:hasAssertion dgn-np:NP46140.RAd2vslhcjVvSWjeWmE_GgXpPfNoXylSvKKyoKnu5In6Y130_assertion;
    np:hasProvenance dgn-np:NP46140.RAd2vslhcjVvSWjeWmE_GgXpPfNoXylSvKKyoKnu5In6Y130_provenance;
    np:hasPublicationInfo dgn-np:NP46140.RAd2vslhcjVvSWjeWmE_GgXpPfNoXylSvKKyoKnu5In6Y130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP46140.RAd2vslhcjVvSWjeWmE_GgXpPfNoXylSvKKyoKnu5In6Y130_assertion a np:Assertion .
  
  dgn-np:NP46140.RAd2vslhcjVvSWjeWmE_GgXpPfNoXylSvKKyoKnu5In6Y130_provenance a np:Provenance .
  
  dgn-np:NP46140.RAd2vslhcjVvSWjeWmE_GgXpPfNoXylSvKKyoKnu5In6Y130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP46140.RAd2vslhcjVvSWjeWmE_GgXpPfNoXylSvKKyoKnu5In6Y130_assertion {
  miriam-gene:1543 a ncit:C16612 .
  
  lld:C0152018 a ncit:C7057 .
  
  dgn-gda:DGNfeffd6158a6497df25ac6f3913029e6e sio:SIO_000628 miriam-gene:1543, lld:C0152018;
    a sio:SIO_001122 .
}

dgn-np:NP46140.RAd2vslhcjVvSWjeWmE_GgXpPfNoXylSvKKyoKnu5In6Y130_provenance {
  dgn-np:NP46140.RAd2vslhcjVvSWjeWmE_GgXpPfNoXylSvKKyoKnu5In6Y130_assertion dcterms:description
      "[The present results suggest that CYP1A1 3' polymorphism may be one of the promising protective factors and its wild gene type may be an indicator for higher susceptibility to esophageal cancer.]. 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:12854128;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP46140.RAd2vslhcjVvSWjeWmE_GgXpPfNoXylSvKKyoKnu5In6Y130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:21+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" .
}