@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP688764.RA1a8B8Y2eqtfzzG9vkiwOdbRuXp3Yqd_HVPCnXQxkh7g> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP688764.RA1a8B8Y2eqtfzzG9vkiwOdbRuXp3Yqd_HVPCnXQxkh7g130_head {
  this: np:hasAssertion dgn-np:NP688764.RA1a8B8Y2eqtfzzG9vkiwOdbRuXp3Yqd_HVPCnXQxkh7g130_assertion;
    np:hasProvenance dgn-np:NP688764.RA1a8B8Y2eqtfzzG9vkiwOdbRuXp3Yqd_HVPCnXQxkh7g130_provenance;
    np:hasPublicationInfo dgn-np:NP688764.RA1a8B8Y2eqtfzzG9vkiwOdbRuXp3Yqd_HVPCnXQxkh7g130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP688764.RA1a8B8Y2eqtfzzG9vkiwOdbRuXp3Yqd_HVPCnXQxkh7g130_assertion a np:Assertion .
  
  dgn-np:NP688764.RA1a8B8Y2eqtfzzG9vkiwOdbRuXp3Yqd_HVPCnXQxkh7g130_provenance a np:Provenance .
  
  dgn-np:NP688764.RA1a8B8Y2eqtfzzG9vkiwOdbRuXp3Yqd_HVPCnXQxkh7g130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP688764.RA1a8B8Y2eqtfzzG9vkiwOdbRuXp3Yqd_HVPCnXQxkh7g130_assertion {
  miriam-gene:6390 a ncit:C16612 .
  
  lld:C0022665 a ncit:C7057 .
  
  dgn-gda:DGNcabc250e3ee00ebd14a7691925023801 sio:SIO_000628 miriam-gene:6390, lld:C0022665;
    a sio:SIO_001121 .
}

dgn-np:NP688764.RA1a8B8Y2eqtfzzG9vkiwOdbRuXp3Yqd_HVPCnXQxkh7g130_provenance {
  dgn-np:NP688764.RA1a8B8Y2eqtfzzG9vkiwOdbRuXp3Yqd_HVPCnXQxkh7g130_assertion dcterms:description
      "[Although detection and management of early tumors is most often associated with a good outcome, based on our initial experience with these patients and our long-term experience with hereditary leiomyomatosis and renal cell carcinoma, we recommend careful surveillance of patients at risk for SDH mutation associated renal cell carcinoma and wide surgical excision of renal tumors.]. 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:23083876;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP688764.RA1a8B8Y2eqtfzzG9vkiwOdbRuXp3Yqd_HVPCnXQxkh7g130_publicationInfo {
  this: dcterms:created "2015-08-25T14:44:35+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}