@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP412580.RA27a3ExolvK18csqfg-6ONNjALRiH4egpHrovszsDtUk> .
@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:NP412580.RA27a3ExolvK18csqfg-6ONNjALRiH4egpHrovszsDtUk130_head {
  this: np:hasAssertion dgn-np:NP412580.RA27a3ExolvK18csqfg-6ONNjALRiH4egpHrovszsDtUk130_assertion ;
    np:hasProvenance dgn-np:NP412580.RA27a3ExolvK18csqfg-6ONNjALRiH4egpHrovszsDtUk130_provenance ;
    np:hasPublicationInfo dgn-np:NP412580.RA27a3ExolvK18csqfg-6ONNjALRiH4egpHrovszsDtUk130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP412580.RA27a3ExolvK18csqfg-6ONNjALRiH4egpHrovszsDtUk130_assertion a np:Assertion .
  dgn-np:NP412580.RA27a3ExolvK18csqfg-6ONNjALRiH4egpHrovszsDtUk130_provenance a np:Provenance .
  dgn-np:NP412580.RA27a3ExolvK18csqfg-6ONNjALRiH4egpHrovszsDtUk130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP412580.RA27a3ExolvK18csqfg-6ONNjALRiH4egpHrovszsDtUk130_assertion {
  miriam-gene:2952 a ncit:C16612 .
  lld:C1140680 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP412580.RA27a3ExolvK18csqfg-6ONNjALRiH4egpHrovszsDtUk130_provenance {
  dgn-np:NP412580.RA27a3ExolvK18csqfg-6ONNjALRiH4egpHrovszsDtUk130_assertion dcterms:description "[We examined the prevalence of GSTM1 and GSTT1 gene deletions, and two GSTP1 polymorphisms in 772 cases with advanced colorectal adenomas (>1 cm, villous elements or high-grade dysplasia) of the distal colon (descending or sigmoid colon or rectum) and 777 sigmoidoscopy negative controls enrolled in the screening arm of the Prostate, Lung, Colorectal, and Ovarian Cancer Screening Trial.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_literature ;
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    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 ;
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}
dgn-np:NP412580.RA27a3ExolvK18csqfg-6ONNjALRiH4egpHrovszsDtUk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:05+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 ;
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}