@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP43015.RAVsmumNLSwJ_gWq3bzZJVNPgsOcJIvYYaPNLgK6w4oL4> .
@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:NP43015.RAVsmumNLSwJ_gWq3bzZJVNPgsOcJIvYYaPNLgK6w4oL4130_head {
  this: np:hasAssertion dgn-np:NP43015.RAVsmumNLSwJ_gWq3bzZJVNPgsOcJIvYYaPNLgK6w4oL4130_assertion;
    np:hasProvenance dgn-np:NP43015.RAVsmumNLSwJ_gWq3bzZJVNPgsOcJIvYYaPNLgK6w4oL4130_provenance;
    np:hasPublicationInfo dgn-np:NP43015.RAVsmumNLSwJ_gWq3bzZJVNPgsOcJIvYYaPNLgK6w4oL4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP43015.RAVsmumNLSwJ_gWq3bzZJVNPgsOcJIvYYaPNLgK6w4oL4130_assertion a np:Assertion .
  
  dgn-np:NP43015.RAVsmumNLSwJ_gWq3bzZJVNPgsOcJIvYYaPNLgK6w4oL4130_provenance a np:Provenance .
  
  dgn-np:NP43015.RAVsmumNLSwJ_gWq3bzZJVNPgsOcJIvYYaPNLgK6w4oL4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP43015.RAVsmumNLSwJ_gWq3bzZJVNPgsOcJIvYYaPNLgK6w4oL4130_assertion {
  miriam-gene:2950 a ncit:C16612 .
  
  lld:C0152018 a ncit:C7057 .
  
  dgn-gda:DGN80561b0ba7aaac27972d5803b9aceee5 sio:SIO_000628 miriam-gene:2950, lld:C0152018;
    a sio:SIO_001122 .
}

dgn-np:NP43015.RAVsmumNLSwJ_gWq3bzZJVNPgsOcJIvYYaPNLgK6w4oL4130_provenance {
  dgn-np:NP43015.RAVsmumNLSwJ_gWq3bzZJVNPgsOcJIvYYaPNLgK6w4oL4130_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:NP43015.RAVsmumNLSwJ_gWq3bzZJVNPgsOcJIvYYaPNLgK6w4oL4130_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" .
}