@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP137558.RAGNYt79eO0lfeufrlmuMJva-cY3LqL_22Zh0RmrPtZ18> .
@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:NP137558.RAGNYt79eO0lfeufrlmuMJva-cY3LqL_22Zh0RmrPtZ18130_head {
  this: np:hasAssertion dgn-np:NP137558.RAGNYt79eO0lfeufrlmuMJva-cY3LqL_22Zh0RmrPtZ18130_assertion;
    np:hasProvenance dgn-np:NP137558.RAGNYt79eO0lfeufrlmuMJva-cY3LqL_22Zh0RmrPtZ18130_provenance;
    np:hasPublicationInfo dgn-np:NP137558.RAGNYt79eO0lfeufrlmuMJva-cY3LqL_22Zh0RmrPtZ18130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP137558.RAGNYt79eO0lfeufrlmuMJva-cY3LqL_22Zh0RmrPtZ18130_assertion a np:Assertion .
  
  dgn-np:NP137558.RAGNYt79eO0lfeufrlmuMJva-cY3LqL_22Zh0RmrPtZ18130_provenance a np:Provenance .
  
  dgn-np:NP137558.RAGNYt79eO0lfeufrlmuMJva-cY3LqL_22Zh0RmrPtZ18130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP137558.RAGNYt79eO0lfeufrlmuMJva-cY3LqL_22Zh0RmrPtZ18130_assertion {
  miriam-gene:2952 a ncit:C16612 .
  
  lld:C0006118 a ncit:C7057 .
  
  dgn-gda:DGNbb46dc8ebfddb373799ce44821cf8445 sio:SIO_000628 miriam-gene:2952, lld:C0006118;
    a sio:SIO_001122 .
}

dgn-np:NP137558.RAGNYt79eO0lfeufrlmuMJva-cY3LqL_22Zh0RmrPtZ18130_provenance {
  dgn-np:NP137558.RAGNYt79eO0lfeufrlmuMJva-cY3LqL_22Zh0RmrPtZ18130_assertion dcterms:description
      "[In patients with anaplastic oligodendroglial tumors, the GSTT1 null genotype may be associated with poor survival, possibly because of modifications in therapy secondary to increased toxicity. This hypothesis is under investigation. In patients with anapl]. 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:20187096;
    prov:wasDerivedFrom dgn-void:gad-20150221;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP137558.RAGNYt79eO0lfeufrlmuMJva-cY3LqL_22Zh0RmrPtZ18130_publicationInfo {
  this: dcterms:created "2015-08-25T14:38:57+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" .
}