@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP171371.RAYi6DIUrMw-VptKlQ6gRP6fuxBZqC3EdETAr3c3cKLiQ> .
@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:NP171371.RAYi6DIUrMw-VptKlQ6gRP6fuxBZqC3EdETAr3c3cKLiQ130_head {
  this: np:hasAssertion dgn-np:NP171371.RAYi6DIUrMw-VptKlQ6gRP6fuxBZqC3EdETAr3c3cKLiQ130_assertion;
    np:hasProvenance dgn-np:NP171371.RAYi6DIUrMw-VptKlQ6gRP6fuxBZqC3EdETAr3c3cKLiQ130_provenance;
    np:hasPublicationInfo dgn-np:NP171371.RAYi6DIUrMw-VptKlQ6gRP6fuxBZqC3EdETAr3c3cKLiQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP171371.RAYi6DIUrMw-VptKlQ6gRP6fuxBZqC3EdETAr3c3cKLiQ130_assertion a np:Assertion .
  
  dgn-np:NP171371.RAYi6DIUrMw-VptKlQ6gRP6fuxBZqC3EdETAr3c3cKLiQ130_provenance a np:Provenance .
  
  dgn-np:NP171371.RAYi6DIUrMw-VptKlQ6gRP6fuxBZqC3EdETAr3c3cKLiQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP171371.RAYi6DIUrMw-VptKlQ6gRP6fuxBZqC3EdETAr3c3cKLiQ130_assertion {
  miriam-gene:672 a ncit:C16612 .
  
  lld:C1458155 a ncit:C7057 .
  
  dgn-gda:DGNf771fc486fefa3c7a5cbe44919d11f0d sio:SIO_000628 miriam-gene:672, lld:C1458155;
    a sio:SIO_001121 .
}

dgn-np:NP171371.RAYi6DIUrMw-VptKlQ6gRP6fuxBZqC3EdETAr3c3cKLiQ130_provenance {
  dgn-np:NP171371.RAYi6DIUrMw-VptKlQ6gRP6fuxBZqC3EdETAr3c3cKLiQ130_assertion dcterms:description
      "[Amplification of AURKA has been detected at higher frequency in tumors from BRCA1 and BRCA2 mutation carriers than in sporadic breast tumors, suggesting that overexpression of AURKA and inactivation of BRCA1 and BRCA2 cooperate during tumor development and progression.]. 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:17627006;
    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:NP171371.RAYi6DIUrMw-VptKlQ6gRP6fuxBZqC3EdETAr3c3cKLiQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:32+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" .
}