@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP755464.RAX_dUc7sMIxXBzAGPyXSvoXgNFTmPksoN4GOFFLEstzk> .
@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:NP755464.RAX_dUc7sMIxXBzAGPyXSvoXgNFTmPksoN4GOFFLEstzk130_head {
  this: np:hasAssertion dgn-np:NP755464.RAX_dUc7sMIxXBzAGPyXSvoXgNFTmPksoN4GOFFLEstzk130_assertion;
    np:hasProvenance dgn-np:NP755464.RAX_dUc7sMIxXBzAGPyXSvoXgNFTmPksoN4GOFFLEstzk130_provenance;
    np:hasPublicationInfo dgn-np:NP755464.RAX_dUc7sMIxXBzAGPyXSvoXgNFTmPksoN4GOFFLEstzk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP755464.RAX_dUc7sMIxXBzAGPyXSvoXgNFTmPksoN4GOFFLEstzk130_assertion a np:Assertion .
  
  dgn-np:NP755464.RAX_dUc7sMIxXBzAGPyXSvoXgNFTmPksoN4GOFFLEstzk130_provenance a np:Provenance .
  
  dgn-np:NP755464.RAX_dUc7sMIxXBzAGPyXSvoXgNFTmPksoN4GOFFLEstzk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP755464.RAX_dUc7sMIxXBzAGPyXSvoXgNFTmPksoN4GOFFLEstzk130_assertion {
  miriam-gene:65266 a ncit:C16612 .
  
  lld:C0019247 a ncit:C7057 .
  
  dgn-gda:DGNb17debbd66da40c2a6d1109b8092e5ea sio:SIO_000628 miriam-gene:65266, lld:C0019247;
    a sio:SIO_001121 .
}

dgn-np:NP755464.RAX_dUc7sMIxXBzAGPyXSvoXgNFTmPksoN4GOFFLEstzk130_provenance {
  dgn-np:NP755464.RAX_dUc7sMIxXBzAGPyXSvoXgNFTmPksoN4GOFFLEstzk130_assertion dcterms:description
      "[The rare autosomal dominant genetic disorder familial hyperkalemia and hypertension which is caused by mutations in WNK4 kinase, is characterized by childhood hyperkalemia and hypercalciuria, and appearance of hypertension in the third to fourth decade.]. 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:20956807;
    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:NP755464.RAX_dUc7sMIxXBzAGPyXSvoXgNFTmPksoN4GOFFLEstzk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:37+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" .
}