@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP988517.RA8K3EKbWP9irDgzF023XCK4PrShmvaYKb0KFc31L3ScI> .
@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:NP988517.RA8K3EKbWP9irDgzF023XCK4PrShmvaYKb0KFc31L3ScI130_head {
  this: np:hasAssertion dgn-np:NP988517.RA8K3EKbWP9irDgzF023XCK4PrShmvaYKb0KFc31L3ScI130_assertion;
    np:hasProvenance dgn-np:NP988517.RA8K3EKbWP9irDgzF023XCK4PrShmvaYKb0KFc31L3ScI130_provenance;
    np:hasPublicationInfo dgn-np:NP988517.RA8K3EKbWP9irDgzF023XCK4PrShmvaYKb0KFc31L3ScI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP988517.RA8K3EKbWP9irDgzF023XCK4PrShmvaYKb0KFc31L3ScI130_assertion a np:Assertion .
  
  dgn-np:NP988517.RA8K3EKbWP9irDgzF023XCK4PrShmvaYKb0KFc31L3ScI130_provenance a np:Provenance .
  
  dgn-np:NP988517.RA8K3EKbWP9irDgzF023XCK4PrShmvaYKb0KFc31L3ScI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP988517.RA8K3EKbWP9irDgzF023XCK4PrShmvaYKb0KFc31L3ScI130_assertion {
  miriam-gene:373156 a ncit:C16612 .
  
  lld:C2239176 a ncit:C7057 .
  
  dgn-gda:DGN4d53d2ee6496cb48657355cf3236ca76 sio:SIO_000628 miriam-gene:373156, lld:C2239176;
    a sio:SIO_001121 .
}

dgn-np:NP988517.RA8K3EKbWP9irDgzF023XCK4PrShmvaYKb0KFc31L3ScI130_provenance {
  dgn-np:NP988517.RA8K3EKbWP9irDgzF023XCK4PrShmvaYKb0KFc31L3ScI130_assertion dcterms:description
      "[The present meta-analysis demonstrated that the GSTM1 and GSTT1 null genotype may be associated with an increased risk of HCC and that individuals having the combination of both defective GST genotypes may be more susceptible to developing HCC.]. 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:24399650;
    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:NP988517.RA8K3EKbWP9irDgzF023XCK4PrShmvaYKb0KFc31L3ScI130_publicationInfo {
  this: dcterms:created "2015-08-25T14:47:46+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" .
}