@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP518286.RAtbPFyEIHLVcUbIiM7AgrCPNyTwY0kPL_NwdiXA3m2kY> .
@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:NP518286.RAtbPFyEIHLVcUbIiM7AgrCPNyTwY0kPL_NwdiXA3m2kY130_head {
  this: np:hasAssertion dgn-np:NP518286.RAtbPFyEIHLVcUbIiM7AgrCPNyTwY0kPL_NwdiXA3m2kY130_assertion;
    np:hasProvenance dgn-np:NP518286.RAtbPFyEIHLVcUbIiM7AgrCPNyTwY0kPL_NwdiXA3m2kY130_provenance;
    np:hasPublicationInfo dgn-np:NP518286.RAtbPFyEIHLVcUbIiM7AgrCPNyTwY0kPL_NwdiXA3m2kY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP518286.RAtbPFyEIHLVcUbIiM7AgrCPNyTwY0kPL_NwdiXA3m2kY130_assertion a np:Assertion .
  
  dgn-np:NP518286.RAtbPFyEIHLVcUbIiM7AgrCPNyTwY0kPL_NwdiXA3m2kY130_provenance a np:Provenance .
  
  dgn-np:NP518286.RAtbPFyEIHLVcUbIiM7AgrCPNyTwY0kPL_NwdiXA3m2kY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP518286.RAtbPFyEIHLVcUbIiM7AgrCPNyTwY0kPL_NwdiXA3m2kY130_assertion {
  miriam-gene:2475 a ncit:C16612 .
  
  lld:C0008626 a ncit:C7057 .
  
  dgn-gda:DGN3c0e3e39099a17d2ac5a634f979bb7af sio:SIO_000628 miriam-gene:2475, lld:C0008626;
    a sio:SIO_001121 .
}

dgn-np:NP518286.RAtbPFyEIHLVcUbIiM7AgrCPNyTwY0kPL_NwdiXA3m2kY130_provenance {
  dgn-np:NP518286.RAtbPFyEIHLVcUbIiM7AgrCPNyTwY0kPL_NwdiXA3m2kY130_assertion dcterms:description
      "[Most notably, the severe chromosomal abnormality did not cause cell death owing to the activation of AKT pathway, including elevated levels of phosphorylated AKT and mammalian target of rapamycin, and nuclear accumulation of cyclin D1, which enabled continuous proliferation of the tetraploid cells.]. 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:16715125;
    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:NP518286.RAtbPFyEIHLVcUbIiM7AgrCPNyTwY0kPL_NwdiXA3m2kY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:08+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" .
}