@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP763703.RADsK9cKK6yEd4mDmQP6STX0TOP9f0FZIIiyIx3Swc_6Y> .
@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:NP763703.RADsK9cKK6yEd4mDmQP6STX0TOP9f0FZIIiyIx3Swc_6Y130_head {
  this: np:hasAssertion dgn-np:NP763703.RADsK9cKK6yEd4mDmQP6STX0TOP9f0FZIIiyIx3Swc_6Y130_assertion;
    np:hasProvenance dgn-np:NP763703.RADsK9cKK6yEd4mDmQP6STX0TOP9f0FZIIiyIx3Swc_6Y130_provenance;
    np:hasPublicationInfo dgn-np:NP763703.RADsK9cKK6yEd4mDmQP6STX0TOP9f0FZIIiyIx3Swc_6Y130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP763703.RADsK9cKK6yEd4mDmQP6STX0TOP9f0FZIIiyIx3Swc_6Y130_assertion a np:Assertion .
  
  dgn-np:NP763703.RADsK9cKK6yEd4mDmQP6STX0TOP9f0FZIIiyIx3Swc_6Y130_provenance a np:Provenance .
  
  dgn-np:NP763703.RADsK9cKK6yEd4mDmQP6STX0TOP9f0FZIIiyIx3Swc_6Y130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP763703.RADsK9cKK6yEd4mDmQP6STX0TOP9f0FZIIiyIx3Swc_6Y130_assertion {
  miriam-gene:898 a ncit:C16612 .
  
  lld:C0026764 a ncit:C7057 .
  
  dgn-gda:DGNc97b538d028c00a9af68b636267d9813 sio:SIO_000628 miriam-gene:898, lld:C0026764;
    a sio:SIO_001121 .
}

dgn-np:NP763703.RADsK9cKK6yEd4mDmQP6STX0TOP9f0FZIIiyIx3Swc_6Y130_provenance {
  dgn-np:NP763703.RADsK9cKK6yEd4mDmQP6STX0TOP9f0FZIIiyIx3Swc_6Y130_assertion dcterms:description
      "[Ectopic over expression of CCNE1 resulted in reduced sensitivity of the MM tumor cells in comparison to the paternal cell line, whereas CCNE1 silencing with siRNA increased the cell sensitivity to seliciclib.]. 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:22558078;
    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:NP763703.RADsK9cKK6yEd4mDmQP6STX0TOP9f0FZIIiyIx3Swc_6Y130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:42+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" .
}