@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP713395.RAVPIJx6TgNM6nqJpSZkO_en7ybXwxnd1CTrrVzwb9KLk> .
@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:NP713395.RAVPIJx6TgNM6nqJpSZkO_en7ybXwxnd1CTrrVzwb9KLk130_head {
  this: np:hasAssertion dgn-np:NP713395.RAVPIJx6TgNM6nqJpSZkO_en7ybXwxnd1CTrrVzwb9KLk130_assertion;
    np:hasProvenance dgn-np:NP713395.RAVPIJx6TgNM6nqJpSZkO_en7ybXwxnd1CTrrVzwb9KLk130_provenance;
    np:hasPublicationInfo dgn-np:NP713395.RAVPIJx6TgNM6nqJpSZkO_en7ybXwxnd1CTrrVzwb9KLk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP713395.RAVPIJx6TgNM6nqJpSZkO_en7ybXwxnd1CTrrVzwb9KLk130_assertion a np:Assertion .
  
  dgn-np:NP713395.RAVPIJx6TgNM6nqJpSZkO_en7ybXwxnd1CTrrVzwb9KLk130_provenance a np:Provenance .
  
  dgn-np:NP713395.RAVPIJx6TgNM6nqJpSZkO_en7ybXwxnd1CTrrVzwb9KLk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP713395.RAVPIJx6TgNM6nqJpSZkO_en7ybXwxnd1CTrrVzwb9KLk130_assertion {
  miriam-gene:2475 a ncit:C16612 .
  
  lld:C1621958 a ncit:C7057 .
  
  dgn-gda:DGN24c21d5a117dd8ea0b50318afd2804b8 sio:SIO_000628 miriam-gene:2475, lld:C1621958;
    a sio:SIO_001121 .
}

dgn-np:NP713395.RAVPIJx6TgNM6nqJpSZkO_en7ybXwxnd1CTrrVzwb9KLk130_provenance {
  dgn-np:NP713395.RAVPIJx6TgNM6nqJpSZkO_en7ybXwxnd1CTrrVzwb9KLk130_assertion dcterms:description
      "[Hyperactivation of the phosphatidylinositol 3-kinase/Akt signaling through disruption of PTEN function is common in glioblastoma multiforme, and these genetic changes are predicted to enhance sensitivity to mammalian target of rapamycin (mTOR) inhibitors such as RAD001 (everolimus).]. 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:18559622;
    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:NP713395.RAVPIJx6TgNM6nqJpSZkO_en7ybXwxnd1CTrrVzwb9KLk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:13+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" .
}