@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP42878.RAkxMgfUpdFKW_ougKd022F500cUV69c-6IMn_s_8nD9U> .
@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:NP42878.RAkxMgfUpdFKW_ougKd022F500cUV69c-6IMn_s_8nD9U130_head {
  this: np:hasAssertion dgn-np:NP42878.RAkxMgfUpdFKW_ougKd022F500cUV69c-6IMn_s_8nD9U130_assertion;
    np:hasProvenance dgn-np:NP42878.RAkxMgfUpdFKW_ougKd022F500cUV69c-6IMn_s_8nD9U130_provenance;
    np:hasPublicationInfo dgn-np:NP42878.RAkxMgfUpdFKW_ougKd022F500cUV69c-6IMn_s_8nD9U130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP42878.RAkxMgfUpdFKW_ougKd022F500cUV69c-6IMn_s_8nD9U130_assertion a np:Assertion .
  
  dgn-np:NP42878.RAkxMgfUpdFKW_ougKd022F500cUV69c-6IMn_s_8nD9U130_provenance a np:Provenance .
  
  dgn-np:NP42878.RAkxMgfUpdFKW_ougKd022F500cUV69c-6IMn_s_8nD9U130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP42878.RAkxMgfUpdFKW_ougKd022F500cUV69c-6IMn_s_8nD9U130_assertion {
  miriam-gene:2952 a ncit:C16612 .
  
  lld:C0023467 a ncit:C7057 .
  
  dgn-gda:DGN0c0588829dfc7db47b6116c0de155439 sio:SIO_000628 miriam-gene:2952, lld:C0023467;
    a sio:SIO_001122 .
}

dgn-np:NP42878.RAkxMgfUpdFKW_ougKd022F500cUV69c-6IMn_s_8nD9U130_provenance {
  dgn-np:NP42878.RAkxMgfUpdFKW_ougKd022F500cUV69c-6IMn_s_8nD9U130_assertion dct:description
      "[We investigated the prognostic significance of genetic polymorphism in glutathione-S transferase mu 1 (GSTM1), glutathione-S transferase theta 1 (GSTT1), NAD(P)H:quinone oxidoreductase (NQO1) and myeloperoxidase (MPO), the products of which are associated with drug metabolism as well as with detoxication, in 193 patients with de novo acute myeloid leukemia (AML) other than M3.]. 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:11840286;
    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:NP42878.RAkxMgfUpdFKW_ougKd022F500cUV69c-6IMn_s_8nD9U130_publicationInfo {
  this: dct:created "2014-10-02T12:32:19+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" .
}