@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP50745.RAYFTviTbubr1KUl4pJ_3Uc2rHdDYCVw9xW8FGrF3StYw> .
@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:NP50745.RAYFTviTbubr1KUl4pJ_3Uc2rHdDYCVw9xW8FGrF3StYw130_head {
  this: np:hasAssertion dgn-np:NP50745.RAYFTviTbubr1KUl4pJ_3Uc2rHdDYCVw9xW8FGrF3StYw130_assertion;
    np:hasProvenance dgn-np:NP50745.RAYFTviTbubr1KUl4pJ_3Uc2rHdDYCVw9xW8FGrF3StYw130_provenance;
    np:hasPublicationInfo dgn-np:NP50745.RAYFTviTbubr1KUl4pJ_3Uc2rHdDYCVw9xW8FGrF3StYw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP50745.RAYFTviTbubr1KUl4pJ_3Uc2rHdDYCVw9xW8FGrF3StYw130_assertion a np:Assertion .
  
  dgn-np:NP50745.RAYFTviTbubr1KUl4pJ_3Uc2rHdDYCVw9xW8FGrF3StYw130_provenance a np:Provenance .
  
  dgn-np:NP50745.RAYFTviTbubr1KUl4pJ_3Uc2rHdDYCVw9xW8FGrF3StYw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP50745.RAYFTviTbubr1KUl4pJ_3Uc2rHdDYCVw9xW8FGrF3StYw130_assertion {
  miriam-gene:7018 a ncit:C16612 .
  
  lld:C0023891 a ncit:C7057 .
  
  dgn-gda:DGN0c459fa7988763fec3301c6d39d6146b sio:SIO_000628 miriam-gene:7018, lld:C0023891;
    a sio:SIO_001122 .
}

dgn-np:NP50745.RAYFTviTbubr1KUl4pJ_3Uc2rHdDYCVw9xW8FGrF3StYw130_provenance {
  dgn-np:NP50745.RAYFTviTbubr1KUl4pJ_3Uc2rHdDYCVw9xW8FGrF3StYw130_assertion dcterms: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:NP50745.RAYFTviTbubr1KUl4pJ_3Uc2rHdDYCVw9xW8FGrF3StYw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:23+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" .
}