@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1354532.RApzhQD6fynntJ1ONI5A_pBGOz3Ne-J1bvCEJkxc4kv9s> .
@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/v4.0.0/void/> .

dgn-np:NP1354532.RApzhQD6fynntJ1ONI5A_pBGOz3Ne-J1bvCEJkxc4kv9s130_head {
  this: np:hasAssertion dgn-np:NP1354532.RApzhQD6fynntJ1ONI5A_pBGOz3Ne-J1bvCEJkxc4kv9s130_assertion;
    np:hasProvenance dgn-np:NP1354532.RApzhQD6fynntJ1ONI5A_pBGOz3Ne-J1bvCEJkxc4kv9s130_provenance;
    np:hasPublicationInfo dgn-np:NP1354532.RApzhQD6fynntJ1ONI5A_pBGOz3Ne-J1bvCEJkxc4kv9s130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1354532.RApzhQD6fynntJ1ONI5A_pBGOz3Ne-J1bvCEJkxc4kv9s130_assertion a np:Assertion .
  
  dgn-np:NP1354532.RApzhQD6fynntJ1ONI5A_pBGOz3Ne-J1bvCEJkxc4kv9s130_provenance a np:Provenance .
  
  dgn-np:NP1354532.RApzhQD6fynntJ1ONI5A_pBGOz3Ne-J1bvCEJkxc4kv9s130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1354532.RApzhQD6fynntJ1ONI5A_pBGOz3Ne-J1bvCEJkxc4kv9s130_assertion {
  miriam-gene:5972 a ncit:C16612 .
  
  lld:C2936861 a ncit:C7057 .
  
  dgn-gda:DGN097737dd1aaeda33f69a1ba534bbde68 sio:SIO_000628 miriam-gene:5972, lld:C2936861;
    a sio:SIO_001121 .
}

dgn-np:NP1354532.RApzhQD6fynntJ1ONI5A_pBGOz3Ne-J1bvCEJkxc4kv9s130_provenance {
  dgn-np:NP1354532.RApzhQD6fynntJ1ONI5A_pBGOz3Ne-J1bvCEJkxc4kv9s130_assertion dcterms:description
      "[The syndrome of apparent mineralocorticoid excess (AME) is a heritable form of hypertension due to an inborn error of cortisol metabolism and is characterized by hypokalemia and low renin levels despite subnormal or normal levels of aldosterone and other known mineralocorticoids.]. 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:8732999;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1354532.RApzhQD6fynntJ1ONI5A_pBGOz3Ne-J1bvCEJkxc4kv9s130_publicationInfo {
  this: dcterms:created "2016-05-13T12:52:00+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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}