@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1248635.RAIR4dQ3ZWjaV3rFpFsulwH2W3xUnBH2DTJnHiTk2nfUQ> .
@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/v4.0.0/void/> .

dgn-np:NP1248635.RAIR4dQ3ZWjaV3rFpFsulwH2W3xUnBH2DTJnHiTk2nfUQ130_head {
  this: np:hasAssertion dgn-np:NP1248635.RAIR4dQ3ZWjaV3rFpFsulwH2W3xUnBH2DTJnHiTk2nfUQ130_assertion;
    np:hasProvenance dgn-np:NP1248635.RAIR4dQ3ZWjaV3rFpFsulwH2W3xUnBH2DTJnHiTk2nfUQ130_provenance;
    np:hasPublicationInfo dgn-np:NP1248635.RAIR4dQ3ZWjaV3rFpFsulwH2W3xUnBH2DTJnHiTk2nfUQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1248635.RAIR4dQ3ZWjaV3rFpFsulwH2W3xUnBH2DTJnHiTk2nfUQ130_assertion a np:Assertion .
  
  dgn-np:NP1248635.RAIR4dQ3ZWjaV3rFpFsulwH2W3xUnBH2DTJnHiTk2nfUQ130_provenance a np:Provenance .
  
  dgn-np:NP1248635.RAIR4dQ3ZWjaV3rFpFsulwH2W3xUnBH2DTJnHiTk2nfUQ130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1248635.RAIR4dQ3ZWjaV3rFpFsulwH2W3xUnBH2DTJnHiTk2nfUQ130_assertion {
  miriam-gene:2952 a ncit:C16612 .
  
  lld:C3539909 a ncit:C7057 .
  
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    a sio:SIO_001121 .
}

dgn-np:NP1248635.RAIR4dQ3ZWjaV3rFpFsulwH2W3xUnBH2DTJnHiTk2nfUQ130_provenance {
  dgn-np:NP1248635.RAIR4dQ3ZWjaV3rFpFsulwH2W3xUnBH2DTJnHiTk2nfUQ130_assertion dcterms:description
      "[In analyzing GSTM1, GSTT1, and GSTP1 sequence variation, we observed other common functional variants that may be candidates for associated studies of diseases related to GST genes (e.g., cancer, cardiovascular disease, and allergy).]. 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:25515186;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1248635.RAIR4dQ3ZWjaV3rFpFsulwH2W3xUnBH2DTJnHiTk2nfUQ130_publicationInfo {
  this: dcterms:created "2016-05-13T12:51:12+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>,
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
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}