@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP669913.RAOxW1s-d9MYd1ldsleS3HAof_DC9lvQ6vhn0Ey2Q_E_g> .
@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/v3.0.0/void/> .
dgn-np:NP669913.RAOxW1s-d9MYd1ldsleS3HAof_DC9lvQ6vhn0Ey2Q_E_g130_head {
  this: np:hasAssertion dgn-np:NP669913.RAOxW1s-d9MYd1ldsleS3HAof_DC9lvQ6vhn0Ey2Q_E_g130_assertion ;
    np:hasProvenance dgn-np:NP669913.RAOxW1s-d9MYd1ldsleS3HAof_DC9lvQ6vhn0Ey2Q_E_g130_provenance ;
    np:hasPublicationInfo dgn-np:NP669913.RAOxW1s-d9MYd1ldsleS3HAof_DC9lvQ6vhn0Ey2Q_E_g130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP669913.RAOxW1s-d9MYd1ldsleS3HAof_DC9lvQ6vhn0Ey2Q_E_g130_assertion a np:Assertion .
  dgn-np:NP669913.RAOxW1s-d9MYd1ldsleS3HAof_DC9lvQ6vhn0Ey2Q_E_g130_provenance a np:Provenance .
  dgn-np:NP669913.RAOxW1s-d9MYd1ldsleS3HAof_DC9lvQ6vhn0Ey2Q_E_g130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP669913.RAOxW1s-d9MYd1ldsleS3HAof_DC9lvQ6vhn0Ey2Q_E_g130_assertion {
  miriam-gene:5972 a ncit:C16612 .
  lld:C0264639 a ncit:C7057 .
  dgn-gda:DGN910c4f01238ce684bfd6fe07a837098d sio:SIO_000628 miriam-gene:5972 , lld:C0264639 ;
    a sio:SIO_001122 .
}
dgn-np:NP669913.RAOxW1s-d9MYd1ldsleS3HAof_DC9lvQ6vhn0Ey2Q_E_g130_provenance {
  dgn-np:NP669913.RAOxW1s-d9MYd1ldsleS3HAof_DC9lvQ6vhn0Ey2Q_E_g130_assertion dcterms:description "[The aim of the study was to investigate allele and genotype frequencies of the -344C/T polymorphism, located in the promoter region of the aldosterone synthase gene, in 83 patients with idiopathic low renin hypertension characterized by an increased aldosterone to renin ratio, including both patients with low renin essential hypertension (n=53) and subjects with idiopathic hyperaldosteronism (n=30), compared with 78 patients with normal to high renin essential hypertension and 126 normotensive control subjects.]. 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:11587161 ;
    prov:wasDerivedFrom dgn-void:befree-20150227 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP669913.RAOxW1s-d9MYd1ldsleS3HAof_DC9lvQ6vhn0Ey2Q_E_g130_publicationInfo {
  this: dcterms:created "2015-08-25T14:44:22+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 "v3.0.0.0" .
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}