@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP887171.RA9jni9Hfyf6_XFW2QVzNrdA7_PYhogXFZo0ZL0fuvDhQ> .
@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:NP887171.RA9jni9Hfyf6_XFW2QVzNrdA7_PYhogXFZo0ZL0fuvDhQ130_head {
  this: np:hasAssertion dgn-np:NP887171.RA9jni9Hfyf6_XFW2QVzNrdA7_PYhogXFZo0ZL0fuvDhQ130_assertion;
    np:hasProvenance dgn-np:NP887171.RA9jni9Hfyf6_XFW2QVzNrdA7_PYhogXFZo0ZL0fuvDhQ130_provenance;
    np:hasPublicationInfo dgn-np:NP887171.RA9jni9Hfyf6_XFW2QVzNrdA7_PYhogXFZo0ZL0fuvDhQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP887171.RA9jni9Hfyf6_XFW2QVzNrdA7_PYhogXFZo0ZL0fuvDhQ130_assertion a np:Assertion .
  
  dgn-np:NP887171.RA9jni9Hfyf6_XFW2QVzNrdA7_PYhogXFZo0ZL0fuvDhQ130_provenance a np:Provenance .
  
  dgn-np:NP887171.RA9jni9Hfyf6_XFW2QVzNrdA7_PYhogXFZo0ZL0fuvDhQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP887171.RA9jni9Hfyf6_XFW2QVzNrdA7_PYhogXFZo0ZL0fuvDhQ130_assertion {
  miriam-gene:4306 a ncit:C16612 .
  
  lld:C0001627 a ncit:C7057 .
  
  dgn-gda:DGNce0fe1dc86270e44e0ac01e89502f042 sio:SIO_000628 miriam-gene:4306, lld:C0001627;
    a sio:SIO_001121 .
}

dgn-np:NP887171.RA9jni9Hfyf6_XFW2QVzNrdA7_PYhogXFZo0ZL0fuvDhQ130_provenance {
  dgn-np:NP887171.RA9jni9Hfyf6_XFW2QVzNrdA7_PYhogXFZo0ZL0fuvDhQ130_assertion dcterms:description
      "[We provide an overview and diagnostic approach to apparent mineralocorticoid excess, glucocorticoid remediable aldosteronism, familial hyperaldosteronism type 2, Liddle's syndrome, Gordon's syndrome, activating mutations of the mineralocorticoid receptor, generalized glucocorticoid resistance and hypertensive forms of congenital adrenal hyperplasia.]. 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:21494136;
    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:NP887171.RA9jni9Hfyf6_XFW2QVzNrdA7_PYhogXFZo0ZL0fuvDhQ130_publicationInfo {
  this: dcterms:created "2016-05-13T12:48:26+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" .
}