@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP42923.RAy0K2m139chTyDxueJmL3Y-feo08hRib5KvU74AmsYA8> .
@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:NP42923.RAy0K2m139chTyDxueJmL3Y-feo08hRib5KvU74AmsYA8130_head {
  this: np:hasAssertion dgn-np:NP42923.RAy0K2m139chTyDxueJmL3Y-feo08hRib5KvU74AmsYA8130_assertion;
    np:hasProvenance dgn-np:NP42923.RAy0K2m139chTyDxueJmL3Y-feo08hRib5KvU74AmsYA8130_provenance;
    np:hasPublicationInfo dgn-np:NP42923.RAy0K2m139chTyDxueJmL3Y-feo08hRib5KvU74AmsYA8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP42923.RAy0K2m139chTyDxueJmL3Y-feo08hRib5KvU74AmsYA8130_assertion a np:Assertion .
  
  dgn-np:NP42923.RAy0K2m139chTyDxueJmL3Y-feo08hRib5KvU74AmsYA8130_provenance a np:Provenance .
  
  dgn-np:NP42923.RAy0K2m139chTyDxueJmL3Y-feo08hRib5KvU74AmsYA8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP42923.RAy0K2m139chTyDxueJmL3Y-feo08hRib5KvU74AmsYA8130_assertion {
  miriam-gene:2950 a ncit:C16612 .
  
  lld:C0546837 a ncit:C7057 .
  
  dgn-gda:DGNb19c7d924bf54c5bff6c435610f12d1d sio:SIO_000628 miriam-gene:2950, lld:C0546837;
    a sio:SIO_001122 .
}

dgn-np:NP42923.RAy0K2m139chTyDxueJmL3Y-feo08hRib5KvU74AmsYA8130_provenance {
  dgn-np:NP42923.RAy0K2m139chTyDxueJmL3Y-feo08hRib5KvU74AmsYA8130_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. mEH slow allele variant, associated with the progression of esophageal precancerous lesions, may contribute to the high susceptibility to esophageal carcinoma.]. 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:NP42923.RAy0K2m139chTyDxueJmL3Y-feo08hRib5KvU74AmsYA8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:19+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" .
}