@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP465179.RACs3njhKqRFf6lmj0tWzmosPnKv9Wc9DVCRaEnGMMyms> .
@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:NP465179.RACs3njhKqRFf6lmj0tWzmosPnKv9Wc9DVCRaEnGMMyms130_head {
  this: np:hasAssertion dgn-np:NP465179.RACs3njhKqRFf6lmj0tWzmosPnKv9Wc9DVCRaEnGMMyms130_assertion;
    np:hasProvenance dgn-np:NP465179.RACs3njhKqRFf6lmj0tWzmosPnKv9Wc9DVCRaEnGMMyms130_provenance;
    np:hasPublicationInfo dgn-np:NP465179.RACs3njhKqRFf6lmj0tWzmosPnKv9Wc9DVCRaEnGMMyms130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP465179.RACs3njhKqRFf6lmj0tWzmosPnKv9Wc9DVCRaEnGMMyms130_assertion a np:Assertion .
  
  dgn-np:NP465179.RACs3njhKqRFf6lmj0tWzmosPnKv9Wc9DVCRaEnGMMyms130_provenance a np:Provenance .
  
  dgn-np:NP465179.RACs3njhKqRFf6lmj0tWzmosPnKv9Wc9DVCRaEnGMMyms130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP465179.RACs3njhKqRFf6lmj0tWzmosPnKv9Wc9DVCRaEnGMMyms130_assertion {
  miriam-gene:1956 a ncit:C16612 .
  
  lld:C0035335 a ncit:C7057 .
  
  dgn-gda:DGNd54f06fb13b80f02a9749c50f3045310 sio:SIO_000628 miriam-gene:1956, lld:C0035335;
    a sio:SIO_001121 .
}

dgn-np:NP465179.RACs3njhKqRFf6lmj0tWzmosPnKv9Wc9DVCRaEnGMMyms130_provenance {
  dgn-np:NP465179.RACs3njhKqRFf6lmj0tWzmosPnKv9Wc9DVCRaEnGMMyms130_assertion dcterms:description
      "[This review covers traditional histologic based classification of infiltrating glial neoplasms together with molecular abnormalities of these tumors involving p53, epidermal growth factor receptor, the retinoblastoma pathway, platelet derived growth factor receptor, genetic losses on chromosome 10, and loss of heterozygosity on chromosomes 1p and 19q.]. 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:12963964;
    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:NP465179.RACs3njhKqRFf6lmj0tWzmosPnKv9Wc9DVCRaEnGMMyms130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:39+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" .
}