@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP714423.RADKpJCpiFgSeOCB0ezG9b_1LZZ6ko0C5N6VC3L2npFH4> .
@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:NP714423.RADKpJCpiFgSeOCB0ezG9b_1LZZ6ko0C5N6VC3L2npFH4130_head {
  this: np:hasAssertion dgn-np:NP714423.RADKpJCpiFgSeOCB0ezG9b_1LZZ6ko0C5N6VC3L2npFH4130_assertion;
    np:hasProvenance dgn-np:NP714423.RADKpJCpiFgSeOCB0ezG9b_1LZZ6ko0C5N6VC3L2npFH4130_provenance;
    np:hasPublicationInfo dgn-np:NP714423.RADKpJCpiFgSeOCB0ezG9b_1LZZ6ko0C5N6VC3L2npFH4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP714423.RADKpJCpiFgSeOCB0ezG9b_1LZZ6ko0C5N6VC3L2npFH4130_assertion a np:Assertion .
  
  dgn-np:NP714423.RADKpJCpiFgSeOCB0ezG9b_1LZZ6ko0C5N6VC3L2npFH4130_provenance a np:Provenance .
  
  dgn-np:NP714423.RADKpJCpiFgSeOCB0ezG9b_1LZZ6ko0C5N6VC3L2npFH4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP714423.RADKpJCpiFgSeOCB0ezG9b_1LZZ6ko0C5N6VC3L2npFH4130_assertion {
  miriam-gene:5376 a ncit:C16612 .
  
  lld:C0279702 a ncit:C7057 .
  
  dgn-gda:DGNed6020a66f088f57f1e6b42dd9e26bb0 sio:SIO_000628 miriam-gene:5376, lld:C0279702;
    a sio:SIO_001121 .
}

dgn-np:NP714423.RADKpJCpiFgSeOCB0ezG9b_1LZZ6ko0C5N6VC3L2npFH4130_provenance {
  dgn-np:NP714423.RADKpJCpiFgSeOCB0ezG9b_1LZZ6ko0C5N6VC3L2npFH4130_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:NP714423.RADKpJCpiFgSeOCB0ezG9b_1LZZ6ko0C5N6VC3L2npFH4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:14+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" .
}