@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1194495.RAIeDxHvXg4czs1_ynB1xZt0v4kz9Y98hoQvJB-keHaEE> .
@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:NP1194495.RAIeDxHvXg4czs1_ynB1xZt0v4kz9Y98hoQvJB-keHaEE130_head {
  this: np:hasAssertion dgn-np:NP1194495.RAIeDxHvXg4czs1_ynB1xZt0v4kz9Y98hoQvJB-keHaEE130_assertion;
    np:hasProvenance dgn-np:NP1194495.RAIeDxHvXg4czs1_ynB1xZt0v4kz9Y98hoQvJB-keHaEE130_provenance;
    np:hasPublicationInfo dgn-np:NP1194495.RAIeDxHvXg4czs1_ynB1xZt0v4kz9Y98hoQvJB-keHaEE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1194495.RAIeDxHvXg4czs1_ynB1xZt0v4kz9Y98hoQvJB-keHaEE130_assertion a np:Assertion .
  
  dgn-np:NP1194495.RAIeDxHvXg4czs1_ynB1xZt0v4kz9Y98hoQvJB-keHaEE130_provenance a np:Provenance .
  
  dgn-np:NP1194495.RAIeDxHvXg4czs1_ynB1xZt0v4kz9Y98hoQvJB-keHaEE130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1194495.RAIeDxHvXg4czs1_ynB1xZt0v4kz9Y98hoQvJB-keHaEE130_assertion {
  miriam-gene:4255 a ncit:C16612 .
  
  lld:C0017638 a ncit:C7057 .
  
  dgn-gda:DGNea9071cb5dcc8a055eb2531443d8da28 sio:SIO_000628 miriam-gene:4255, lld:C0017638;
    a sio:SIO_001121 .
}

dgn-np:NP1194495.RAIeDxHvXg4czs1_ynB1xZt0v4kz9Y98hoQvJB-keHaEE130_provenance {
  dgn-np:NP1194495.RAIeDxHvXg4czs1_ynB1xZt0v4kz9Y98hoQvJB-keHaEE130_assertion dcterms:description
      "[Loss of 1p and 19q was seen in only 4 patients although hemizygous loss of 1p36 occurred in 20%.The findings support reports that IDH1/2 mutations and MGMT methylation can be used in addition to tumour grade and clinical factors to predict survival in patients with recurrent high grade gliomas when treated with any of the therapy regimes used.]. 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:24952577;
    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:NP1194495.RAIeDxHvXg4czs1_ynB1xZt0v4kz9Y98hoQvJB-keHaEE130_publicationInfo {
  this: dcterms:created "2016-05-13T12:50:47+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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}