@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP891911.RAKEzttfs2UIxZjRWHuq2iyTZFKA_gj3XsE2JYjINf3cc> .
@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:NP891911.RAKEzttfs2UIxZjRWHuq2iyTZFKA_gj3XsE2JYjINf3cc130_head {
  this: np:hasAssertion dgn-np:NP891911.RAKEzttfs2UIxZjRWHuq2iyTZFKA_gj3XsE2JYjINf3cc130_assertion;
    np:hasProvenance dgn-np:NP891911.RAKEzttfs2UIxZjRWHuq2iyTZFKA_gj3XsE2JYjINf3cc130_provenance;
    np:hasPublicationInfo dgn-np:NP891911.RAKEzttfs2UIxZjRWHuq2iyTZFKA_gj3XsE2JYjINf3cc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP891911.RAKEzttfs2UIxZjRWHuq2iyTZFKA_gj3XsE2JYjINf3cc130_assertion a np:Assertion .
  
  dgn-np:NP891911.RAKEzttfs2UIxZjRWHuq2iyTZFKA_gj3XsE2JYjINf3cc130_provenance a np:Provenance .
  
  dgn-np:NP891911.RAKEzttfs2UIxZjRWHuq2iyTZFKA_gj3XsE2JYjINf3cc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP891911.RAKEzttfs2UIxZjRWHuq2iyTZFKA_gj3XsE2JYjINf3cc130_assertion {
  miriam-gene:28956 a ncit:C16612 .
  
  lld:C0007134 a ncit:C7057 .
  
  dgn-gda:DGN913a053932874351aa3f819b0bd625b3 sio:SIO_000628 miriam-gene:28956, lld:C0007134;
    a sio:SIO_001121 .
}

dgn-np:NP891911.RAKEzttfs2UIxZjRWHuq2iyTZFKA_gj3XsE2JYjINf3cc130_provenance {
  dgn-np:NP891911.RAKEzttfs2UIxZjRWHuq2iyTZFKA_gj3XsE2JYjINf3cc130_assertion dcterms:description
      "[The majority of these markers clustered in three regions that have been suggested to be involved in the development of RCC, namely the p25 region, where the von Hippel Lindau (VHL) gene is located; the p21 region, which has been identified as a common region of overlap (SRO) of heterozygous deletions; and the p14 region, which is the location of the constitutional t(3;8) breakpoint occurring in an RCC family.]. 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:8824727;
    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:NP891911.RAKEzttfs2UIxZjRWHuq2iyTZFKA_gj3XsE2JYjINf3cc130_publicationInfo {
  this: dcterms:created "2015-08-25T14:46:44+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" .
}