@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP250588.RABJx3SWbtqPbhFcPLdky4XlnC8yL2K_8sLq5XawisUUA> .
@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:NP250588.RABJx3SWbtqPbhFcPLdky4XlnC8yL2K_8sLq5XawisUUA130_head {
  this: np:hasAssertion dgn-np:NP250588.RABJx3SWbtqPbhFcPLdky4XlnC8yL2K_8sLq5XawisUUA130_assertion;
    np:hasProvenance dgn-np:NP250588.RABJx3SWbtqPbhFcPLdky4XlnC8yL2K_8sLq5XawisUUA130_provenance;
    np:hasPublicationInfo dgn-np:NP250588.RABJx3SWbtqPbhFcPLdky4XlnC8yL2K_8sLq5XawisUUA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP250588.RABJx3SWbtqPbhFcPLdky4XlnC8yL2K_8sLq5XawisUUA130_assertion a np:Assertion .
  
  dgn-np:NP250588.RABJx3SWbtqPbhFcPLdky4XlnC8yL2K_8sLq5XawisUUA130_provenance a np:Provenance .
  
  dgn-np:NP250588.RABJx3SWbtqPbhFcPLdky4XlnC8yL2K_8sLq5XawisUUA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP250588.RABJx3SWbtqPbhFcPLdky4XlnC8yL2K_8sLq5XawisUUA130_assertion {
  miriam-gene:23291 a ncit:C16612 .
  
  lld:C0585442 a ncit:C7057 .
  
  dgn-gda:DGNce9a320ac38e2222fac23bc2461e5cde sio:SIO_000628 miriam-gene:23291, lld:C0585442;
    a sio:SIO_001121 .
}

dgn-np:NP250588.RABJx3SWbtqPbhFcPLdky4XlnC8yL2K_8sLq5XawisUUA130_provenance {
  dgn-np:NP250588.RABJx3SWbtqPbhFcPLdky4XlnC8yL2K_8sLq5XawisUUA130_assertion dcterms:description
      "[We also investigated whether there was an association between TP53 mutation and centrosome aberrations in the generation of chromosomal aneuploidy in OS in four OS cell lines (HOS, SAOS2, U2OS, and MG63) and in a subset of seven tumors.]. 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:12850370;
    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:NP250588.RABJx3SWbtqPbhFcPLdky4XlnC8yL2K_8sLq5XawisUUA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:20+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" .
}