@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP258844.RABGQCsPbzUtCriSTi2e7GeRh04-NqH6T5r3qAKRUvvBA> .
@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:NP258844.RABGQCsPbzUtCriSTi2e7GeRh04-NqH6T5r3qAKRUvvBA130_head {
  this: np:hasAssertion dgn-np:NP258844.RABGQCsPbzUtCriSTi2e7GeRh04-NqH6T5r3qAKRUvvBA130_assertion;
    np:hasProvenance dgn-np:NP258844.RABGQCsPbzUtCriSTi2e7GeRh04-NqH6T5r3qAKRUvvBA130_provenance;
    np:hasPublicationInfo dgn-np:NP258844.RABGQCsPbzUtCriSTi2e7GeRh04-NqH6T5r3qAKRUvvBA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP258844.RABGQCsPbzUtCriSTi2e7GeRh04-NqH6T5r3qAKRUvvBA130_assertion a np:Assertion .
  
  dgn-np:NP258844.RABGQCsPbzUtCriSTi2e7GeRh04-NqH6T5r3qAKRUvvBA130_provenance a np:Provenance .
  
  dgn-np:NP258844.RABGQCsPbzUtCriSTi2e7GeRh04-NqH6T5r3qAKRUvvBA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP258844.RABGQCsPbzUtCriSTi2e7GeRh04-NqH6T5r3qAKRUvvBA130_assertion {
  miriam-gene:1571 a ncit:C16612 .
  
  lld:C0006826 a ncit:C7057 .
  
  dgn-gda:DGN15617de343a76e702e394e57e45fcafb sio:SIO_000628 miriam-gene:1571, lld:C0006826;
    a sio:SIO_001121 .
}

dgn-np:NP258844.RABGQCsPbzUtCriSTi2e7GeRh04-NqH6T5r3qAKRUvvBA130_provenance {
  dgn-np:NP258844.RABGQCsPbzUtCriSTi2e7GeRh04-NqH6T5r3qAKRUvvBA130_assertion dcterms:description
      "[Multiple regression analyses of data, with metabolic polymorphisms, smoking habits, alcohol consumption, age, gender, and family history of cancer as independent variables, showed that smoking habits, and possibly the CYP2E1 variant genotypes, were the main factors explaining the variance of both SCE and HFC.]. 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:12113772;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP258844.RABGQCsPbzUtCriSTi2e7GeRh04-NqH6T5r3qAKRUvvBA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:24+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" .
}