@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1274757.RAjU-tApS8e9NJ6D5szO2xiTJmNu0Rm-XGxqtt-krSCok> .
@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:NP1274757.RAjU-tApS8e9NJ6D5szO2xiTJmNu0Rm-XGxqtt-krSCok130_head {
  this: np:hasAssertion dgn-np:NP1274757.RAjU-tApS8e9NJ6D5szO2xiTJmNu0Rm-XGxqtt-krSCok130_assertion;
    np:hasProvenance dgn-np:NP1274757.RAjU-tApS8e9NJ6D5szO2xiTJmNu0Rm-XGxqtt-krSCok130_provenance;
    np:hasPublicationInfo dgn-np:NP1274757.RAjU-tApS8e9NJ6D5szO2xiTJmNu0Rm-XGxqtt-krSCok130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1274757.RAjU-tApS8e9NJ6D5szO2xiTJmNu0Rm-XGxqtt-krSCok130_assertion a np:Assertion .
  
  dgn-np:NP1274757.RAjU-tApS8e9NJ6D5szO2xiTJmNu0Rm-XGxqtt-krSCok130_provenance a np:Provenance .
  
  dgn-np:NP1274757.RAjU-tApS8e9NJ6D5szO2xiTJmNu0Rm-XGxqtt-krSCok130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1274757.RAjU-tApS8e9NJ6D5szO2xiTJmNu0Rm-XGxqtt-krSCok130_assertion {
  miriam-gene:79798 a ncit:C16612 .
  
  lld:C0524620 a ncit:C7057 .
  
  dgn-gda:DGNea77af9d2dd8c0f2f1db718b1df2ce2f sio:SIO_000628 miriam-gene:79798, lld:C0524620;
    a sio:SIO_001121 .
}

dgn-np:NP1274757.RAjU-tApS8e9NJ6D5szO2xiTJmNu0Rm-XGxqtt-krSCok130_provenance {
  dgn-np:NP1274757.RAjU-tApS8e9NJ6D5szO2xiTJmNu0Rm-XGxqtt-krSCok130_assertion dcterms:description
      "[Additional cohorts of patients with primary aldosteronism and metabolic syndrome, particularly African Americans, should be screened for ARMC5 sequence variants because these may underlie part of the known increased predisposition of African Americans to low renin 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:25822102;
    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:NP1274757.RAjU-tApS8e9NJ6D5szO2xiTJmNu0Rm-XGxqtt-krSCok130_publicationInfo {
  this: dcterms:created "2016-05-13T12:51:24+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: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" .
}