@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP437692.RApPV8k7x8kOi34wvejeMW5A6zqu0fbt3GBPN3e7n9Bl0> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP437692.RApPV8k7x8kOi34wvejeMW5A6zqu0fbt3GBPN3e7n9Bl0130_head {
  this: np:hasAssertion dgn-np:NP437692.RApPV8k7x8kOi34wvejeMW5A6zqu0fbt3GBPN3e7n9Bl0130_assertion;
    np:hasProvenance dgn-np:NP437692.RApPV8k7x8kOi34wvejeMW5A6zqu0fbt3GBPN3e7n9Bl0130_provenance;
    np:hasPublicationInfo dgn-np:NP437692.RApPV8k7x8kOi34wvejeMW5A6zqu0fbt3GBPN3e7n9Bl0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP437692.RApPV8k7x8kOi34wvejeMW5A6zqu0fbt3GBPN3e7n9Bl0130_assertion a np:Assertion .
  
  dgn-np:NP437692.RApPV8k7x8kOi34wvejeMW5A6zqu0fbt3GBPN3e7n9Bl0130_provenance a np:Provenance .
  
  dgn-np:NP437692.RApPV8k7x8kOi34wvejeMW5A6zqu0fbt3GBPN3e7n9Bl0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP437692.RApPV8k7x8kOi34wvejeMW5A6zqu0fbt3GBPN3e7n9Bl0130_assertion {
  miriam-gene:2944 a ncit:C16612 .
  
  lld:C0023448 a ncit:C7057 .
  
  dgn-gda:DGN9f7107f155ad111d0ca144ad22d2a391 sio:SIO_000628 miriam-gene:2944, lld:C0023448;
    a sio:SIO_001121 .
}

dgn-np:NP437692.RApPV8k7x8kOi34wvejeMW5A6zqu0fbt3GBPN3e7n9Bl0130_provenance {
  dgn-np:NP437692.RApPV8k7x8kOi34wvejeMW5A6zqu0fbt3GBPN3e7n9Bl0130_assertion dcterms:description
      "[Significantly increased frequencies of GSTM1 null genotype (M0), GSTT1 null genotype (T0) and GST double null genotype (T0M0) were observed in the both ALL and AML cases as compared to controls.]. 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:23725116;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP437692.RApPV8k7x8kOi34wvejeMW5A6zqu0fbt3GBPN3e7n9Bl0130_publicationInfo {
  this: dcterms:created "2015-08-25T14:41:55+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}