@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP231495.RATQHc4NwMF6HPDacwliWGD-K_B08gX5AxISi9S0hgtTs> .
@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:NP231495.RATQHc4NwMF6HPDacwliWGD-K_B08gX5AxISi9S0hgtTs130_head {
  this: np:hasAssertion dgn-np:NP231495.RATQHc4NwMF6HPDacwliWGD-K_B08gX5AxISi9S0hgtTs130_assertion;
    np:hasProvenance dgn-np:NP231495.RATQHc4NwMF6HPDacwliWGD-K_B08gX5AxISi9S0hgtTs130_provenance;
    np:hasPublicationInfo dgn-np:NP231495.RATQHc4NwMF6HPDacwliWGD-K_B08gX5AxISi9S0hgtTs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP231495.RATQHc4NwMF6HPDacwliWGD-K_B08gX5AxISi9S0hgtTs130_assertion a np:Assertion .
  
  dgn-np:NP231495.RATQHc4NwMF6HPDacwliWGD-K_B08gX5AxISi9S0hgtTs130_provenance a np:Provenance .
  
  dgn-np:NP231495.RATQHc4NwMF6HPDacwliWGD-K_B08gX5AxISi9S0hgtTs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP231495.RATQHc4NwMF6HPDacwliWGD-K_B08gX5AxISi9S0hgtTs130_assertion {
  miriam-gene:5728 a ncit:C16612 .
  
  lld:C0017636 a ncit:C7057 .
  
  dgn-gda:DGNdd1bbc589a52323cd6b249db8517dc95 sio:SIO_000628 miriam-gene:5728, lld:C0017636;
    a sio:SIO_001121 .
}

dgn-np:NP231495.RATQHc4NwMF6HPDacwliWGD-K_B08gX5AxISi9S0hgtTs130_provenance {
  dgn-np:NP231495.RATQHc4NwMF6HPDacwliWGD-K_B08gX5AxISi9S0hgtTs130_assertion dcterms:description
      "[None of these five glioblastomas showed amplification of the EGFR or PDGFRA genes, while three of the tumors, including two with NRAS and one with BRAF mutation, demonstrated PTEN missense mutations or loss of PTEN mRNA expression.]. 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:15517309;
    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:NP231495.RATQHc4NwMF6HPDacwliWGD-K_B08gX5AxISi9S0hgtTs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:10+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" .
}