@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP524084.RA5JPCKJcqdd7LQIPcSykSZDmLkV_enPtWIa9EMRidwFc> .
@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:NP524084.RA5JPCKJcqdd7LQIPcSykSZDmLkV_enPtWIa9EMRidwFc130_head {
  this: np:hasAssertion dgn-np:NP524084.RA5JPCKJcqdd7LQIPcSykSZDmLkV_enPtWIa9EMRidwFc130_assertion;
    np:hasProvenance dgn-np:NP524084.RA5JPCKJcqdd7LQIPcSykSZDmLkV_enPtWIa9EMRidwFc130_provenance;
    np:hasPublicationInfo dgn-np:NP524084.RA5JPCKJcqdd7LQIPcSykSZDmLkV_enPtWIa9EMRidwFc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP524084.RA5JPCKJcqdd7LQIPcSykSZDmLkV_enPtWIa9EMRidwFc130_assertion a np:Assertion .
  
  dgn-np:NP524084.RA5JPCKJcqdd7LQIPcSykSZDmLkV_enPtWIa9EMRidwFc130_provenance a np:Provenance .
  
  dgn-np:NP524084.RA5JPCKJcqdd7LQIPcSykSZDmLkV_enPtWIa9EMRidwFc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP524084.RA5JPCKJcqdd7LQIPcSykSZDmLkV_enPtWIa9EMRidwFc130_assertion {
  miriam-gene:2944 a ncit:C16612 .
  
  lld:C0029925 a ncit:C7057 .
  
  dgn-gda:DGN1d850bc0532d26f90d1acfaf618bb996 sio:SIO_000628 miriam-gene:2944, lld:C0029925;
    a sio:SIO_001121 .
}

dgn-np:NP524084.RA5JPCKJcqdd7LQIPcSykSZDmLkV_enPtWIa9EMRidwFc130_provenance {
  dgn-np:NP524084.RA5JPCKJcqdd7LQIPcSykSZDmLkV_enPtWIa9EMRidwFc130_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;
    sio:SIO_000772 miriam-pubmed:16030123;
    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:NP524084.RA5JPCKJcqdd7LQIPcSykSZDmLkV_enPtWIa9EMRidwFc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:14+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" .
}