@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP317185.RAcACyIqXZvZ_QmO1CrCREeOUY5MNfxEeOysFjiAN5BZ8> .
@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:NP317185.RAcACyIqXZvZ_QmO1CrCREeOUY5MNfxEeOysFjiAN5BZ8130_head {
  this: np:hasAssertion dgn-np:NP317185.RAcACyIqXZvZ_QmO1CrCREeOUY5MNfxEeOysFjiAN5BZ8130_assertion;
    np:hasProvenance dgn-np:NP317185.RAcACyIqXZvZ_QmO1CrCREeOUY5MNfxEeOysFjiAN5BZ8130_provenance;
    np:hasPublicationInfo dgn-np:NP317185.RAcACyIqXZvZ_QmO1CrCREeOUY5MNfxEeOysFjiAN5BZ8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP317185.RAcACyIqXZvZ_QmO1CrCREeOUY5MNfxEeOysFjiAN5BZ8130_assertion a np:Assertion .
  
  dgn-np:NP317185.RAcACyIqXZvZ_QmO1CrCREeOUY5MNfxEeOysFjiAN5BZ8130_provenance a np:Provenance .
  
  dgn-np:NP317185.RAcACyIqXZvZ_QmO1CrCREeOUY5MNfxEeOysFjiAN5BZ8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP317185.RAcACyIqXZvZ_QmO1CrCREeOUY5MNfxEeOysFjiAN5BZ8130_assertion {
  miriam-gene:595 a ncit:C16612 .
  
  lld:C0007134 a ncit:C7057 .
  
  dgn-gda:DGN1509e6ab1ed83a530146755f6cf5f534 sio:SIO_000628 miriam-gene:595, lld:C0007134;
    a sio:SIO_001121 .
}

dgn-np:NP317185.RAcACyIqXZvZ_QmO1CrCREeOUY5MNfxEeOysFjiAN5BZ8130_provenance {
  dgn-np:NP317185.RAcACyIqXZvZ_QmO1CrCREeOUY5MNfxEeOysFjiAN5BZ8130_assertion dcterms:description
      "[In this case, the correlation of the microscopic findings with changes in CCND1 gene associated to CCND1 overexpression in both components suggest that the ChRCC would have originated from the preexisting oncocytoma.]. 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:16337860;
    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:NP317185.RAcACyIqXZvZ_QmO1CrCREeOUY5MNfxEeOysFjiAN5BZ8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:04+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" .
}