@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1251038.RAYtBAHX8dM8o-MNzaT4rMnA6OrgFzGZ_nuerPufot-1A> .
@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:NP1251038.RAYtBAHX8dM8o-MNzaT4rMnA6OrgFzGZ_nuerPufot-1A130_head {
  this: np:hasAssertion dgn-np:NP1251038.RAYtBAHX8dM8o-MNzaT4rMnA6OrgFzGZ_nuerPufot-1A130_assertion;
    np:hasProvenance dgn-np:NP1251038.RAYtBAHX8dM8o-MNzaT4rMnA6OrgFzGZ_nuerPufot-1A130_provenance;
    np:hasPublicationInfo dgn-np:NP1251038.RAYtBAHX8dM8o-MNzaT4rMnA6OrgFzGZ_nuerPufot-1A130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1251038.RAYtBAHX8dM8o-MNzaT4rMnA6OrgFzGZ_nuerPufot-1A130_assertion a np:Assertion .
  
  dgn-np:NP1251038.RAYtBAHX8dM8o-MNzaT4rMnA6OrgFzGZ_nuerPufot-1A130_provenance a np:Provenance .
  
  dgn-np:NP1251038.RAYtBAHX8dM8o-MNzaT4rMnA6OrgFzGZ_nuerPufot-1A130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1251038.RAYtBAHX8dM8o-MNzaT4rMnA6OrgFzGZ_nuerPufot-1A130_assertion {
  miriam-gene:5443 a ncit:C16612 .
  
  lld:C1384514 a ncit:C7057 .
  
  dgn-gda:DGNa75d7cc2062c12d4f7017817c2f0705c sio:SIO_000628 miriam-gene:5443, lld:C1384514;
    a sio:SIO_001121 .
}

dgn-np:NP1251038.RAYtBAHX8dM8o-MNzaT4rMnA6OrgFzGZ_nuerPufot-1A130_provenance {
  dgn-np:NP1251038.RAYtBAHX8dM8o-MNzaT4rMnA6OrgFzGZ_nuerPufot-1A130_assertion dcterms:description
      "[In the present review, we critically analyse the current means used to diagnose PA along with the role that ACTH, aberrant receptor expression and genetic alterations may exert, and provide evidence for an increased prevalence of aldosterone dysregulation in patients with essential hypertension and pre-hypertension.]. 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:25538205;
    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:NP1251038.RAYtBAHX8dM8o-MNzaT4rMnA6OrgFzGZ_nuerPufot-1A130_publicationInfo {
  this: dcterms:created "2016-05-13T12:51:13+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" .
}