@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP528283.RAFOPz9WPBZbc6sBwxJtaPq_4XhUfzJgOgfTa4e5Rp_p4> .
@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:NP528283.RAFOPz9WPBZbc6sBwxJtaPq_4XhUfzJgOgfTa4e5Rp_p4130_head {
  this: np:hasAssertion dgn-np:NP528283.RAFOPz9WPBZbc6sBwxJtaPq_4XhUfzJgOgfTa4e5Rp_p4130_assertion;
    np:hasProvenance dgn-np:NP528283.RAFOPz9WPBZbc6sBwxJtaPq_4XhUfzJgOgfTa4e5Rp_p4130_provenance;
    np:hasPublicationInfo dgn-np:NP528283.RAFOPz9WPBZbc6sBwxJtaPq_4XhUfzJgOgfTa4e5Rp_p4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP528283.RAFOPz9WPBZbc6sBwxJtaPq_4XhUfzJgOgfTa4e5Rp_p4130_assertion a np:Assertion .
  
  dgn-np:NP528283.RAFOPz9WPBZbc6sBwxJtaPq_4XhUfzJgOgfTa4e5Rp_p4130_provenance a np:Provenance .
  
  dgn-np:NP528283.RAFOPz9WPBZbc6sBwxJtaPq_4XhUfzJgOgfTa4e5Rp_p4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP528283.RAFOPz9WPBZbc6sBwxJtaPq_4XhUfzJgOgfTa4e5Rp_p4130_assertion {
  miriam-gene:7428 a ncit:C16612 .
  
  lld:C1334978 a ncit:C7057 .
  
  dgn-gda:DGNa9d6e5177bf3f460d2bd95d78f1e859d sio:SIO_000628 miriam-gene:7428, lld:C1334978;
    a sio:SIO_001121 .
}

dgn-np:NP528283.RAFOPz9WPBZbc6sBwxJtaPq_4XhUfzJgOgfTa4e5Rp_p4130_provenance {
  dgn-np:NP528283.RAFOPz9WPBZbc6sBwxJtaPq_4XhUfzJgOgfTa4e5Rp_p4130_assertion dcterms:description
      "[As VHL mutations are common in sporadic clear cell renal cell carcinoma, but not papillary renal cell carcinoma, we asked whether there is an association between VHL status and primary cilia in vivo.]. 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:18660794;
    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:NP528283.RAFOPz9WPBZbc6sBwxJtaPq_4XhUfzJgOgfTa4e5Rp_p4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:19+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" .
}