@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP52094.RAroeGnWbtla8Laxv0_93NdYPAJYKEgyaiuFpfELT2LLg> .
@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:NP52094.RAroeGnWbtla8Laxv0_93NdYPAJYKEgyaiuFpfELT2LLg130_head {
  this: np:hasAssertion dgn-np:NP52094.RAroeGnWbtla8Laxv0_93NdYPAJYKEgyaiuFpfELT2LLg130_assertion;
    np:hasProvenance dgn-np:NP52094.RAroeGnWbtla8Laxv0_93NdYPAJYKEgyaiuFpfELT2LLg130_provenance;
    np:hasPublicationInfo dgn-np:NP52094.RAroeGnWbtla8Laxv0_93NdYPAJYKEgyaiuFpfELT2LLg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP52094.RAroeGnWbtla8Laxv0_93NdYPAJYKEgyaiuFpfELT2LLg130_assertion a np:Assertion .
  
  dgn-np:NP52094.RAroeGnWbtla8Laxv0_93NdYPAJYKEgyaiuFpfELT2LLg130_provenance a np:Provenance .
  
  dgn-np:NP52094.RAroeGnWbtla8Laxv0_93NdYPAJYKEgyaiuFpfELT2LLg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP52094.RAroeGnWbtla8Laxv0_93NdYPAJYKEgyaiuFpfELT2LLg130_assertion {
  miriam-gene:6338 a ncit:C16612 .
  
  lld:C0020538 a ncit:C7057 .
  
  dgn-gda:DGN6c4df38e238b768f0b135badebf0ad51 sio:SIO_000628 miriam-gene:6338, lld:C0020538;
    a sio:SIO_001122 .
}

dgn-np:NP52094.RAroeGnWbtla8Laxv0_93NdYPAJYKEgyaiuFpfELT2LLg130_provenance {
  dgn-np:NP52094.RAroeGnWbtla8Laxv0_93NdYPAJYKEgyaiuFpfELT2LLg130_assertion dcterms:description
      "[ At least 9% of Finnish patients with hypertension admitted to a specialized center carry genetic variants of beta and gammaENaC, a three times higher prevalence than in the normotensive individuals or in random healthy controls. Patients with the variant alleles showed an increased urinary potassium excretion rate in relation to their renin levels.]. 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:15661075;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP52094.RAroeGnWbtla8Laxv0_93NdYPAJYKEgyaiuFpfELT2LLg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:24+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" .
}