@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP700542.RAqX8eKywa3VjkqN2Ujv6vo_x4sSxUxa6fj8JYqw40Qyw> .
@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:NP700542.RAqX8eKywa3VjkqN2Ujv6vo_x4sSxUxa6fj8JYqw40Qyw130_head {
  this: np:hasAssertion dgn-np:NP700542.RAqX8eKywa3VjkqN2Ujv6vo_x4sSxUxa6fj8JYqw40Qyw130_assertion;
    np:hasProvenance dgn-np:NP700542.RAqX8eKywa3VjkqN2Ujv6vo_x4sSxUxa6fj8JYqw40Qyw130_provenance;
    np:hasPublicationInfo dgn-np:NP700542.RAqX8eKywa3VjkqN2Ujv6vo_x4sSxUxa6fj8JYqw40Qyw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP700542.RAqX8eKywa3VjkqN2Ujv6vo_x4sSxUxa6fj8JYqw40Qyw130_assertion a np:Assertion .
  
  dgn-np:NP700542.RAqX8eKywa3VjkqN2Ujv6vo_x4sSxUxa6fj8JYqw40Qyw130_provenance a np:Provenance .
  
  dgn-np:NP700542.RAqX8eKywa3VjkqN2Ujv6vo_x4sSxUxa6fj8JYqw40Qyw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP700542.RAqX8eKywa3VjkqN2Ujv6vo_x4sSxUxa6fj8JYqw40Qyw130_assertion {
  miriam-gene:6559 a ncit:C16612 .
  
  lld:C0220666 a ncit:C7057 .
  
  dgn-gda:DGNc2357980f65f7ac94fc37b7ec495d673 sio:SIO_000628 miriam-gene:6559, lld:C0220666;
    a sio:SIO_001121 .
}

dgn-np:NP700542.RAqX8eKywa3VjkqN2Ujv6vo_x4sSxUxa6fj8JYqw40Qyw130_provenance {
  dgn-np:NP700542.RAqX8eKywa3VjkqN2Ujv6vo_x4sSxUxa6fj8JYqw40Qyw130_assertion dcterms:description
      "[It has been appreciated for several years that WNK kinases affect NCC expression, following the discovery that mutations in WNK genes cause Gordon syndrome (pseudohypoaldosteronism type II), although the precise molecular mechanisms were unclear.]. 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:21088576;
    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:NP700542.RAqX8eKywa3VjkqN2Ujv6vo_x4sSxUxa6fj8JYqw40Qyw130_publicationInfo {
  this: dcterms:created "2015-08-25T14:44:42+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" .
}