@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP474741.RA6jsDFOm-fNBB7VX4St6op9mpSvjsDEUnffldT2KUTEE> .
@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:NP474741.RA6jsDFOm-fNBB7VX4St6op9mpSvjsDEUnffldT2KUTEE130_head {
  this: np:hasAssertion dgn-np:NP474741.RA6jsDFOm-fNBB7VX4St6op9mpSvjsDEUnffldT2KUTEE130_assertion;
    np:hasProvenance dgn-np:NP474741.RA6jsDFOm-fNBB7VX4St6op9mpSvjsDEUnffldT2KUTEE130_provenance;
    np:hasPublicationInfo dgn-np:NP474741.RA6jsDFOm-fNBB7VX4St6op9mpSvjsDEUnffldT2KUTEE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP474741.RA6jsDFOm-fNBB7VX4St6op9mpSvjsDEUnffldT2KUTEE130_assertion a np:Assertion .
  
  dgn-np:NP474741.RA6jsDFOm-fNBB7VX4St6op9mpSvjsDEUnffldT2KUTEE130_provenance a np:Provenance .
  
  dgn-np:NP474741.RA6jsDFOm-fNBB7VX4St6op9mpSvjsDEUnffldT2KUTEE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP474741.RA6jsDFOm-fNBB7VX4St6op9mpSvjsDEUnffldT2KUTEE130_assertion {
  miriam-gene:3417 a ncit:C16612 .
  
  lld:C0004114 a ncit:C7057 .
  
  dgn-gda:DGNb70e162f6a081a7a985ee2cb2eded511 sio:SIO_000628 miriam-gene:3417, lld:C0004114;
    a sio:SIO_001121 .
}

dgn-np:NP474741.RA6jsDFOm-fNBB7VX4St6op9mpSvjsDEUnffldT2KUTEE130_provenance {
  dgn-np:NP474741.RA6jsDFOm-fNBB7VX4St6op9mpSvjsDEUnffldT2KUTEE130_assertion dcterms:description
      "[In non 1p/19q codeleted LGGs, we demonstrated that (i) 11p loss is associated with astrocytoma phenotype and has an independent negative prognostic value, and (ii) 19q loss diminished the favorable prognostic value of IDH mutation.]. 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:24335697;
    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:NP474741.RA6jsDFOm-fNBB7VX4St6op9mpSvjsDEUnffldT2KUTEE130_publicationInfo {
  this: dcterms:created "2015-08-25T14:42:20+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" .
}