@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP57565.RA5JTOrn4vBAdD-TK3PSM_Nf63hN4p-nXhPt49vR0YFwE> .
@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 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:NP57565.RA5JTOrn4vBAdD-TK3PSM_Nf63hN4p-nXhPt49vR0YFwE130_head {
  this: np:hasAssertion dgn-np:NP57565.RA5JTOrn4vBAdD-TK3PSM_Nf63hN4p-nXhPt49vR0YFwE130_assertion;
    np:hasProvenance dgn-np:NP57565.RA5JTOrn4vBAdD-TK3PSM_Nf63hN4p-nXhPt49vR0YFwE130_provenance;
    np:hasPublicationInfo dgn-np:NP57565.RA5JTOrn4vBAdD-TK3PSM_Nf63hN4p-nXhPt49vR0YFwE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP57565.RA5JTOrn4vBAdD-TK3PSM_Nf63hN4p-nXhPt49vR0YFwE130_assertion a np:Assertion .
  
  dgn-np:NP57565.RA5JTOrn4vBAdD-TK3PSM_Nf63hN4p-nXhPt49vR0YFwE130_provenance a np:Provenance .
  
  dgn-np:NP57565.RA5JTOrn4vBAdD-TK3PSM_Nf63hN4p-nXhPt49vR0YFwE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP57565.RA5JTOrn4vBAdD-TK3PSM_Nf63hN4p-nXhPt49vR0YFwE130_assertion {
  miriam-gene:3240 a ncit:C16612 .
  
  lld:C0023891 a ncit:C7057 .
  
  dgn-gda:DGN9d94796508aa669cc9d80cac1ffa303e sio:SIO_000628 miriam-gene:3240, lld:C0023891;
    a sio:SIO_001122 .
}

dgn-np:NP57565.RA5JTOrn4vBAdD-TK3PSM_Nf63hN4p-nXhPt49vR0YFwE130_provenance {
  dgn-np:NP57565.RA5JTOrn4vBAdD-TK3PSM_Nf63hN4p-nXhPt49vR0YFwE130_assertion dct:description
      "[The TC patients exhibited a significantly higher frequency of the liver glutathione-S-transferase GST1*0 allele, whereas the GST1*2 frequency was two times higher in the control subjects than in the TC patients (0.2522 and 0.0953, respectively). The TC and control groups showed statistically significant differences in the frequencies of the following]. 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:11436564;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP57565.RA5JTOrn4vBAdD-TK3PSM_Nf63hN4p-nXhPt49vR0YFwE130_publicationInfo {
  this: dct:created "2014-10-02T12:32:27+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}