@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP133215.RAQ2hOt7eA8bFfa_rJE2d0eQGfOc7e03gK_njkm_fSElQ> .
@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:NP133215.RAQ2hOt7eA8bFfa_rJE2d0eQGfOc7e03gK_njkm_fSElQ130_head {
  this: np:hasAssertion dgn-np:NP133215.RAQ2hOt7eA8bFfa_rJE2d0eQGfOc7e03gK_njkm_fSElQ130_assertion;
    np:hasProvenance dgn-np:NP133215.RAQ2hOt7eA8bFfa_rJE2d0eQGfOc7e03gK_njkm_fSElQ130_provenance;
    np:hasPublicationInfo dgn-np:NP133215.RAQ2hOt7eA8bFfa_rJE2d0eQGfOc7e03gK_njkm_fSElQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP133215.RAQ2hOt7eA8bFfa_rJE2d0eQGfOc7e03gK_njkm_fSElQ130_assertion a np:Assertion .
  
  dgn-np:NP133215.RAQ2hOt7eA8bFfa_rJE2d0eQGfOc7e03gK_njkm_fSElQ130_provenance a np:Provenance .
  
  dgn-np:NP133215.RAQ2hOt7eA8bFfa_rJE2d0eQGfOc7e03gK_njkm_fSElQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP133215.RAQ2hOt7eA8bFfa_rJE2d0eQGfOc7e03gK_njkm_fSElQ130_assertion {
  miriam-gene:3779 a ncit:C16612 .
  
  lld:C0027719 a ncit:C7057 .
  
  dgn-gda:DGN1b11c56a0543b5e1c00013708e69e913 sio:SIO_000628 miriam-gene:3779, lld:C0027719;
    a sio:SIO_001122 .
}

dgn-np:NP133215.RAQ2hOt7eA8bFfa_rJE2d0eQGfOc7e03gK_njkm_fSElQ130_provenance {
  dgn-np:NP133215.RAQ2hOt7eA8bFfa_rJE2d0eQGfOc7e03gK_njkm_fSElQ130_assertion dcterms:description
      "[Common KCNMB1 gain-of-function variant Glu65Lys influences GFR, and 65Lys carriers exhibit not only elevated baseline GFR, but also more rapid GFR decline (and consequent development of renal failure) in CKD. The results suggest that profiling patients at]. 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:20861615;
    prov:wasDerivedFrom dgn-void:gad-20150221;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP133215.RAQ2hOt7eA8bFfa_rJE2d0eQGfOc7e03gK_njkm_fSElQ130_publicationInfo {
  this: dcterms:created "2015-08-25T14:38:54+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" .
}