@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP193850.RAHCSYEBNDGrXeogW8DNKiCSsUlf1e-9uBJYE4mPC9fbM> .
@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:NP193850.RAHCSYEBNDGrXeogW8DNKiCSsUlf1e-9uBJYE4mPC9fbM130_head {
  this: np:hasAssertion dgn-np:NP193850.RAHCSYEBNDGrXeogW8DNKiCSsUlf1e-9uBJYE4mPC9fbM130_assertion ;
    np:hasProvenance dgn-np:NP193850.RAHCSYEBNDGrXeogW8DNKiCSsUlf1e-9uBJYE4mPC9fbM130_provenance ;
    np:hasPublicationInfo dgn-np:NP193850.RAHCSYEBNDGrXeogW8DNKiCSsUlf1e-9uBJYE4mPC9fbM130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP193850.RAHCSYEBNDGrXeogW8DNKiCSsUlf1e-9uBJYE4mPC9fbM130_assertion a np:Assertion .
  dgn-np:NP193850.RAHCSYEBNDGrXeogW8DNKiCSsUlf1e-9uBJYE4mPC9fbM130_provenance a np:Provenance .
  dgn-np:NP193850.RAHCSYEBNDGrXeogW8DNKiCSsUlf1e-9uBJYE4mPC9fbM130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP193850.RAHCSYEBNDGrXeogW8DNKiCSsUlf1e-9uBJYE4mPC9fbM130_assertion {
  miriam-gene:2944 a ncit:C16612 .
  lld:C0006826 a ncit:C7057 .
  dgn-gda:DGN0c9ad98790f46eeac00c14f005ec1798 sio:SIO_000628 miriam-gene:2944 , lld:C0006826 ;
    a sio:SIO_001121 .
}
dgn-np:NP193850.RAHCSYEBNDGrXeogW8DNKiCSsUlf1e-9uBJYE4mPC9fbM130_provenance {
  dgn-np:NP193850.RAHCSYEBNDGrXeogW8DNKiCSsUlf1e-9uBJYE4mPC9fbM130_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:NP193850.RAHCSYEBNDGrXeogW8DNKiCSsUlf1e-9uBJYE4mPC9fbM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:46+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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}