@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1282452.RArZExKXJ7vymAgP-fJcBIf9juyoXKyqY-o5JULAxFsX8> .
@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:NP1282452.RArZExKXJ7vymAgP-fJcBIf9juyoXKyqY-o5JULAxFsX8130_head {
  this: np:hasAssertion dgn-np:NP1282452.RArZExKXJ7vymAgP-fJcBIf9juyoXKyqY-o5JULAxFsX8130_assertion;
    np:hasProvenance dgn-np:NP1282452.RArZExKXJ7vymAgP-fJcBIf9juyoXKyqY-o5JULAxFsX8130_provenance;
    np:hasPublicationInfo dgn-np:NP1282452.RArZExKXJ7vymAgP-fJcBIf9juyoXKyqY-o5JULAxFsX8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1282452.RArZExKXJ7vymAgP-fJcBIf9juyoXKyqY-o5JULAxFsX8130_assertion a np:Assertion .
  
  dgn-np:NP1282452.RArZExKXJ7vymAgP-fJcBIf9juyoXKyqY-o5JULAxFsX8130_provenance a np:Provenance .
  
  dgn-np:NP1282452.RArZExKXJ7vymAgP-fJcBIf9juyoXKyqY-o5JULAxFsX8130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1282452.RArZExKXJ7vymAgP-fJcBIf9juyoXKyqY-o5JULAxFsX8130_assertion {
  miriam-gene:3417 a ncit:C16612 .
  
  lld:C0751396 a ncit:C7057 .
  
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dgn-np:NP1282452.RArZExKXJ7vymAgP-fJcBIf9juyoXKyqY-o5JULAxFsX8130_provenance {
  dgn-np:NP1282452.RArZExKXJ7vymAgP-fJcBIf9juyoXKyqY-o5JULAxFsX8130_assertion dcterms:description
      "[More recently described biomarkers, including the non-balanced translocation leading to 1p/19q codeletion, promoter hypermethylation of the MGMT gene, mutations of the IDH1 or IDH2 gene, and mutations of FUBP1 (on 1p) or CIC (on 19q), have greatly enhanced our understanding of oligodendroglioma biology, although their diagnostic, prognostic, and predictive roles are less clear.]. 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:25943885;
    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:NP1282452.RArZExKXJ7vymAgP-fJcBIf9juyoXKyqY-o5JULAxFsX8130_publicationInfo {
  this: dcterms:created "2016-05-13T12:51:27+02:00"^^xsd:dateTime;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dcterms:rightsHolder dgn-void:IBIGroup;
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    pav:authoredBy <http://orcid.org/0000-0001-5999-6269>, <http://orcid.org/0000-0002-7534-7661>,
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  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}