@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP166133.RAul9QlRnKoUlV4rrRp1_ge9O6F8m1BRvHlj_eTWHQKz0> .
@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:NP166133.RAul9QlRnKoUlV4rrRp1_ge9O6F8m1BRvHlj_eTWHQKz0130_head {
   this: np:hasAssertion dgn-np:NP166133.RAul9QlRnKoUlV4rrRp1_ge9O6F8m1BRvHlj_eTWHQKz0130_assertion ;
    np:hasProvenance dgn-np:NP166133.RAul9QlRnKoUlV4rrRp1_ge9O6F8m1BRvHlj_eTWHQKz0130_provenance ;
    np:hasPublicationInfo dgn-np:NP166133.RAul9QlRnKoUlV4rrRp1_ge9O6F8m1BRvHlj_eTWHQKz0130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP166133.RAul9QlRnKoUlV4rrRp1_ge9O6F8m1BRvHlj_eTWHQKz0130_assertion a np:Assertion .
  dgn-np:NP166133.RAul9QlRnKoUlV4rrRp1_ge9O6F8m1BRvHlj_eTWHQKz0130_provenance a np:Provenance .
  dgn-np:NP166133.RAul9QlRnKoUlV4rrRp1_ge9O6F8m1BRvHlj_eTWHQKz0130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP166133.RAul9QlRnKoUlV4rrRp1_ge9O6F8m1BRvHlj_eTWHQKz0130_assertion {
   miriam-gene:9 a ncit:C16612 .
  lld:C0006826 a ncit:C7057 .
  dgn-gda:DGNc435220e00bc44a14eacf1fdc3e3cace sio:SIO_000628 miriam-gene:9 , lld:C0006826 ;
    a sio:SIO_001121 .
}
dgn-np:NP166133.RAul9QlRnKoUlV4rrRp1_ge9O6F8m1BRvHlj_eTWHQKz0130_provenance {
   dgn-np:NP166133.RAul9QlRnKoUlV4rrRp1_ge9O6F8m1BRvHlj_eTWHQKz0130_assertion dcterms:description "[These results provide further evidence for the combined effects of genetic polymorphisms in GSTM1, GSTT1, NAT1 and NAT2 on DNA and protein adduct formation in smoking individuals and indicate that, due to the complex carcinogen exposure, simultaneous assessment of multiple genotypes may identify individuals at higher cancer risk.]. 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:11470992 ;
    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:NP166133.RAul9QlRnKoUlV4rrRp1_ge9O6F8m1BRvHlj_eTWHQKz0130_publicationInfo {
   this: dcterms:created "2014-10-02T12:33:30+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" .
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}