@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP46282.RAuGu9GYRkzXIEtRn40UhbpTKWZKZy43uPi3roStcaM4o> .
@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/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-np: <http://rdf.disgenet.org/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .

dgn-np:NP46282.RAuGu9GYRkzXIEtRn40UhbpTKWZKZy43uPi3roStcaM4o130_head {
  this: np:hasAssertion dgn-np:NP46282.RAuGu9GYRkzXIEtRn40UhbpTKWZKZy43uPi3roStcaM4o130_assertion;
    np:hasProvenance dgn-np:NP46282.RAuGu9GYRkzXIEtRn40UhbpTKWZKZy43uPi3roStcaM4o130_provenance;
    np:hasPublicationInfo dgn-np:NP46282.RAuGu9GYRkzXIEtRn40UhbpTKWZKZy43uPi3roStcaM4o130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP46282.RAuGu9GYRkzXIEtRn40UhbpTKWZKZy43uPi3roStcaM4o130_assertion a np:Assertion .
  
  dgn-np:NP46282.RAuGu9GYRkzXIEtRn40UhbpTKWZKZy43uPi3roStcaM4o130_provenance a np:Provenance .
  
  dgn-np:NP46282.RAuGu9GYRkzXIEtRn40UhbpTKWZKZy43uPi3roStcaM4o130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP46282.RAuGu9GYRkzXIEtRn40UhbpTKWZKZy43uPi3roStcaM4o130_assertion {
  miriam-gene:1585 a ncit:C16612 .
  
  lld:C0149721 a ncit:C7057 .
  
  dgn-gda:DGNe285159fbc833fe4880c433aa4a9063b sio:SIO_000628 miriam-gene:1585, lld:C0149721;
    a sio:SIO_001122 .
}

dgn-np:NP46282.RAuGu9GYRkzXIEtRn40UhbpTKWZKZy43uPi3roStcaM4o130_provenance {
  dgn-np:NP46282.RAuGu9GYRkzXIEtRn40UhbpTKWZKZy43uPi3roStcaM4o130_assertion dct:description
      "[ In agreement with previous studies, we found that the TT genotype of T-344C polymorphism of aldosterone synthase gene was associated with significantly higher levels of PRA in normotensive men. In subjects with high PRA, the TT genotype was associated with higher values of the LVMI.]. 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:15223724;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP46282.RAuGu9GYRkzXIEtRn40UhbpTKWZKZy43uPi3roStcaM4o130_publicationInfo {
  this: dct:created "2014-10-02T12:32:21+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}