@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1385630.RAD5T1Ln249xz44SmpCggWpUtBfwFBGinHR84YP16dDNA> .
@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:NP1385630.RAD5T1Ln249xz44SmpCggWpUtBfwFBGinHR84YP16dDNA130_head {
  this: np:hasAssertion dgn-np:NP1385630.RAD5T1Ln249xz44SmpCggWpUtBfwFBGinHR84YP16dDNA130_assertion;
    np:hasProvenance dgn-np:NP1385630.RAD5T1Ln249xz44SmpCggWpUtBfwFBGinHR84YP16dDNA130_provenance;
    np:hasPublicationInfo dgn-np:NP1385630.RAD5T1Ln249xz44SmpCggWpUtBfwFBGinHR84YP16dDNA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1385630.RAD5T1Ln249xz44SmpCggWpUtBfwFBGinHR84YP16dDNA130_assertion a np:Assertion .
  
  dgn-np:NP1385630.RAD5T1Ln249xz44SmpCggWpUtBfwFBGinHR84YP16dDNA130_provenance a np:Provenance .
  
  dgn-np:NP1385630.RAD5T1Ln249xz44SmpCggWpUtBfwFBGinHR84YP16dDNA130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1385630.RAD5T1Ln249xz44SmpCggWpUtBfwFBGinHR84YP16dDNA130_assertion {
  miriam-gene:189 a ncit:C16612 .
  
  lld:C0020538 a ncit:C7057 .
  
  dgn-gda:DGNe3fda91a5bdbd85039b25a15e6830fff sio:SIO_000628 miriam-gene:189, lld:C0020538;
    a sio:SIO_001121 .
}

dgn-np:NP1385630.RAD5T1Ln249xz44SmpCggWpUtBfwFBGinHR84YP16dDNA130_provenance {
  dgn-np:NP1385630.RAD5T1Ln249xz44SmpCggWpUtBfwFBGinHR84YP16dDNA130_assertion dcterms:description
      "[Despite a statistically significant, albeit weak, association between the AGT 235T variant and hypertension that has been confirmed through sensitivity analysis, this finding has to be interpreted with caution, as the methodological weaknesses of the individual studies are likely to have biased the outcome of the meta-analysis.]. 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:9403549;
    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:NP1385630.RAD5T1Ln249xz44SmpCggWpUtBfwFBGinHR84YP16dDNA130_publicationInfo {
  this: dcterms:created "2016-05-13T12:52:14+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" .
}