@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP161919.RAd39fAwZPRVVeD1-Zjru3VX22ecdWrnOxTmh9Pxhur08> .
@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:NP161919.RAd39fAwZPRVVeD1-Zjru3VX22ecdWrnOxTmh9Pxhur08130_head {
  this: np:hasAssertion dgn-np:NP161919.RAd39fAwZPRVVeD1-Zjru3VX22ecdWrnOxTmh9Pxhur08130_assertion;
    np:hasProvenance dgn-np:NP161919.RAd39fAwZPRVVeD1-Zjru3VX22ecdWrnOxTmh9Pxhur08130_provenance;
    np:hasPublicationInfo dgn-np:NP161919.RAd39fAwZPRVVeD1-Zjru3VX22ecdWrnOxTmh9Pxhur08130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP161919.RAd39fAwZPRVVeD1-Zjru3VX22ecdWrnOxTmh9Pxhur08130_assertion a np:Assertion .
  
  dgn-np:NP161919.RAd39fAwZPRVVeD1-Zjru3VX22ecdWrnOxTmh9Pxhur08130_provenance a np:Provenance .
  
  dgn-np:NP161919.RAd39fAwZPRVVeD1-Zjru3VX22ecdWrnOxTmh9Pxhur08130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP161919.RAd39fAwZPRVVeD1-Zjru3VX22ecdWrnOxTmh9Pxhur08130_assertion {
  miriam-gene:3091 a ncit:C16612 .
  
  lld:C0740457 a ncit:C7057 .
  
  dgn-gda:DGN74c1a6e762ce221a3d3f2a2e0551fff4 sio:SIO_000628 miriam-gene:3091, lld:C0740457;
    a sio:SIO_001121 .
}

dgn-np:NP161919.RAd39fAwZPRVVeD1-Zjru3VX22ecdWrnOxTmh9Pxhur08130_provenance {
  dgn-np:NP161919.RAd39fAwZPRVVeD1-Zjru3VX22ecdWrnOxTmh9Pxhur08130_assertion dcterms:description
      "[Clear cell renal cell carcinoma (ccRCC) is the most common form of kidney cancer and is often linked to loss of chromosome 3p, which harbors the VHL tumor suppressor gene, loss of chromosome 14q, which includes HIF1A, and gain of chromosome 5q.]. 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:24332042;
    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:NP161919.RAd39fAwZPRVVeD1-Zjru3VX22ecdWrnOxTmh9Pxhur08130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:27+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" .
}