@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP495901.RAe2AV_RDQHMzAZdAUt92fbisloPHzpxsGsU-djn7lrrs> .
@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/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@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/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .

dgn-np:NP495901.RAe2AV_RDQHMzAZdAUt92fbisloPHzpxsGsU-djn7lrrs130_head {
  this: np:hasAssertion dgn-np:NP495901.RAe2AV_RDQHMzAZdAUt92fbisloPHzpxsGsU-djn7lrrs130_assertion;
    np:hasProvenance dgn-np:NP495901.RAe2AV_RDQHMzAZdAUt92fbisloPHzpxsGsU-djn7lrrs130_provenance;
    np:hasPublicationInfo dgn-np:NP495901.RAe2AV_RDQHMzAZdAUt92fbisloPHzpxsGsU-djn7lrrs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP495901.RAe2AV_RDQHMzAZdAUt92fbisloPHzpxsGsU-djn7lrrs130_assertion a np:Assertion .
  
  dgn-np:NP495901.RAe2AV_RDQHMzAZdAUt92fbisloPHzpxsGsU-djn7lrrs130_provenance a np:Provenance .
  
  dgn-np:NP495901.RAe2AV_RDQHMzAZdAUt92fbisloPHzpxsGsU-djn7lrrs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP495901.RAe2AV_RDQHMzAZdAUt92fbisloPHzpxsGsU-djn7lrrs130_assertion {
  miriam-gene:1029 a ncit:C16612 .
  
  lld:C0028945 a ncit:C7057 .
  
  dgn-gda:DGN7fe29a009adb5acda9441a6224494aee sio:SIO_000628 miriam-gene:1029, lld:C0028945;
    a sio:SIO_001121 .
}

dgn-np:NP495901.RAe2AV_RDQHMzAZdAUt92fbisloPHzpxsGsU-djn7lrrs130_provenance {
  dgn-np:NP495901.RAe2AV_RDQHMzAZdAUt92fbisloPHzpxsGsU-djn7lrrs130_assertion dcterms:description
      "[To verify the prognostic implications of the statuses of chromosome 1p and 19q and the expressions of p53, p16 and GFAP in oligodendrogliomas, we investigated these parameters and correlated the results with patient outcome.]. 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:17319279;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP495901.RAe2AV_RDQHMzAZdAUt92fbisloPHzpxsGsU-djn7lrrs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:56+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:disgenetrdf;
    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 "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}