@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP45032.RABMeD7lj8Eh_a6Yl8GytziWygaDrwRbfBzEzMtn1IV9I> .
@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:NP45032.RABMeD7lj8Eh_a6Yl8GytziWygaDrwRbfBzEzMtn1IV9I130_head {
  this: np:hasAssertion dgn-np:NP45032.RABMeD7lj8Eh_a6Yl8GytziWygaDrwRbfBzEzMtn1IV9I130_assertion;
    np:hasProvenance dgn-np:NP45032.RABMeD7lj8Eh_a6Yl8GytziWygaDrwRbfBzEzMtn1IV9I130_provenance;
    np:hasPublicationInfo dgn-np:NP45032.RABMeD7lj8Eh_a6Yl8GytziWygaDrwRbfBzEzMtn1IV9I130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP45032.RABMeD7lj8Eh_a6Yl8GytziWygaDrwRbfBzEzMtn1IV9I130_assertion a np:Assertion .
  
  dgn-np:NP45032.RABMeD7lj8Eh_a6Yl8GytziWygaDrwRbfBzEzMtn1IV9I130_provenance a np:Provenance .
  
  dgn-np:NP45032.RABMeD7lj8Eh_a6Yl8GytziWygaDrwRbfBzEzMtn1IV9I130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP45032.RABMeD7lj8Eh_a6Yl8GytziWygaDrwRbfBzEzMtn1IV9I130_assertion {
  miriam-gene:2052 a ncit:C16612 .
  
  lld:C0242379 a ncit:C7057 .
  
  dgn-gda:DGNef466bed9e3ad1201e524a15d9c16e32 sio:SIO_000628 miriam-gene:2052, lld:C0242379;
    a sio:SIO_001122 .
}

dgn-np:NP45032.RABMeD7lj8Eh_a6Yl8GytziWygaDrwRbfBzEzMtn1IV9I130_provenance {
  dgn-np:NP45032.RABMeD7lj8Eh_a6Yl8GytziWygaDrwRbfBzEzMtn1IV9I130_assertion dcterms:description
      "[We did not find a consistent modification of the carcinogenic effect of smoking according to mEH polymorphism, although the risk of lung cancer decreased among never smokers with high mEH activity and among heavy smokers with the exon 3 His/His genotype.]. 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:12141066;
    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:NP45032.RABMeD7lj8Eh_a6Yl8GytziWygaDrwRbfBzEzMtn1IV9I130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:20+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" .
}