@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP206539.RAHXHYGWVXSdAeTGWR3y3N97osyYKjVQE6nbnJyAtEjQI> .
@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:NP206539.RAHXHYGWVXSdAeTGWR3y3N97osyYKjVQE6nbnJyAtEjQI130_head {
  this: np:hasAssertion dgn-np:NP206539.RAHXHYGWVXSdAeTGWR3y3N97osyYKjVQE6nbnJyAtEjQI130_assertion ;
    np:hasProvenance dgn-np:NP206539.RAHXHYGWVXSdAeTGWR3y3N97osyYKjVQE6nbnJyAtEjQI130_provenance ;
    np:hasPublicationInfo dgn-np:NP206539.RAHXHYGWVXSdAeTGWR3y3N97osyYKjVQE6nbnJyAtEjQI130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP206539.RAHXHYGWVXSdAeTGWR3y3N97osyYKjVQE6nbnJyAtEjQI130_assertion a np:Assertion .
  dgn-np:NP206539.RAHXHYGWVXSdAeTGWR3y3N97osyYKjVQE6nbnJyAtEjQI130_provenance a np:Provenance .
  dgn-np:NP206539.RAHXHYGWVXSdAeTGWR3y3N97osyYKjVQE6nbnJyAtEjQI130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP206539.RAHXHYGWVXSdAeTGWR3y3N97osyYKjVQE6nbnJyAtEjQI130_assertion {
  miriam-gene:2952 a ncit:C16612 .
  lld:C0006826 a ncit:C7057 .
  dgn-gda:DGN64e84e3d86ff5707d9b5ae12b08ca589 sio:SIO_000628 miriam-gene:2952 , lld:C0006826 ;
    a sio:SIO_001121 .
}
dgn-np:NP206539.RAHXHYGWVXSdAeTGWR3y3N97osyYKjVQE6nbnJyAtEjQI130_provenance {
  dgn-np:NP206539.RAHXHYGWVXSdAeTGWR3y3N97osyYKjVQE6nbnJyAtEjQI130_assertion dcterms:description "[Our findings have indicated that the individuals polymorphic for CYP1A1 MspI either with GSTM1 null or with GSTT1 null genotypes revealed an increased risk for UADT cancers than that ascribed to a single susceptible gene among the tobacco users in the population [single gene risk among smokers and chewers, respectively, for CYP1A1 MspI (OR 6.43; 95% CI 3.69-11.21); (OR 10.24; 95% CI 5.95-17.60), GSTM1*0 (OR 3.77; 95% CI 1.94-7.37); (OR 7.97 95% CI 4.10-15.76) and GSTT1*0 (OR 6.95 95% CI 2.88-16.77); (OR 25.83 95% CI 7.78-85.76).]. 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:20012094 ;
    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:NP206539.RAHXHYGWVXSdAeTGWR3y3N97osyYKjVQE6nbnJyAtEjQI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:54+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" .
}