@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP365465.RABIY3_1x15rgLVSnA-etF3g_hVh7iz1W0WWUWFdQthik> .
@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 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:NP365465.RABIY3_1x15rgLVSnA-etF3g_hVh7iz1W0WWUWFdQthik130_head {
  this: np:hasAssertion dgn-np:NP365465.RABIY3_1x15rgLVSnA-etF3g_hVh7iz1W0WWUWFdQthik130_assertion;
    np:hasProvenance dgn-np:NP365465.RABIY3_1x15rgLVSnA-etF3g_hVh7iz1W0WWUWFdQthik130_provenance;
    np:hasPublicationInfo dgn-np:NP365465.RABIY3_1x15rgLVSnA-etF3g_hVh7iz1W0WWUWFdQthik130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP365465.RABIY3_1x15rgLVSnA-etF3g_hVh7iz1W0WWUWFdQthik130_assertion a np:Assertion .
  
  dgn-np:NP365465.RABIY3_1x15rgLVSnA-etF3g_hVh7iz1W0WWUWFdQthik130_provenance a np:Provenance .
  
  dgn-np:NP365465.RABIY3_1x15rgLVSnA-etF3g_hVh7iz1W0WWUWFdQthik130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP365465.RABIY3_1x15rgLVSnA-etF3g_hVh7iz1W0WWUWFdQthik130_assertion {
  miriam-gene:190 a ncit:C16612 .
  
  lld:C0279702 a ncit:C7057 .
  
  dgn-gda:DGN6ed91c53e7dfd94baadc82227fb31cc6 sio:SIO_000628 miriam-gene:190, lld:C0279702;
    a sio:SIO_001121 .
}

dgn-np:NP365465.RABIY3_1x15rgLVSnA-etF3g_hVh7iz1W0WWUWFdQthik130_provenance {
  dgn-np:NP365465.RABIY3_1x15rgLVSnA-etF3g_hVh7iz1W0WWUWFdQthik130_assertion dcterms:description
      "[The aim of this study was to evaluate the prevalence of chromosome 8q gain in clear cell renal cell carcinoma (CCRCC) and to correlate the findings with tumor phenotype and disease-specific survival (DSS).]. 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:22605478;
    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:NP365465.RABIY3_1x15rgLVSnA-etF3g_hVh7iz1W0WWUWFdQthik130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:34+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 orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}