@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP343908.RA5QHWkWTXVGIXXH6RGCo0PMIcjglKLQdnB0HwbYd4Xb8> .
@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:NP343908.RA5QHWkWTXVGIXXH6RGCo0PMIcjglKLQdnB0HwbYd4Xb8130_head {
  this: np:hasAssertion dgn-np:NP343908.RA5QHWkWTXVGIXXH6RGCo0PMIcjglKLQdnB0HwbYd4Xb8130_assertion;
    np:hasProvenance dgn-np:NP343908.RA5QHWkWTXVGIXXH6RGCo0PMIcjglKLQdnB0HwbYd4Xb8130_provenance;
    np:hasPublicationInfo dgn-np:NP343908.RA5QHWkWTXVGIXXH6RGCo0PMIcjglKLQdnB0HwbYd4Xb8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP343908.RA5QHWkWTXVGIXXH6RGCo0PMIcjglKLQdnB0HwbYd4Xb8130_assertion a np:Assertion .
  
  dgn-np:NP343908.RA5QHWkWTXVGIXXH6RGCo0PMIcjglKLQdnB0HwbYd4Xb8130_provenance a np:Provenance .
  
  dgn-np:NP343908.RA5QHWkWTXVGIXXH6RGCo0PMIcjglKLQdnB0HwbYd4Xb8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP343908.RA5QHWkWTXVGIXXH6RGCo0PMIcjglKLQdnB0HwbYd4Xb8130_assertion {
  miriam-gene:1579 a ncit:C16612 .
  
  lld:C0848548 a ncit:C7057 .
  
  dgn-gda:DGNe487296c24efe833df2c7dde339eb5cb sio:SIO_000628 miriam-gene:1579, lld:C0848548;
    a sio:SIO_001122 .
}

dgn-np:NP343908.RA5QHWkWTXVGIXXH6RGCo0PMIcjglKLQdnB0HwbYd4Xb8130_provenance {
  dgn-np:NP343908.RA5QHWkWTXVGIXXH6RGCo0PMIcjglKLQdnB0HwbYd4Xb8130_assertion dcterms:description
      "[This study tested the hypothesis that the CYP4A11 T8590C polymorphism is associated with higher BP or clinical outcomes in 732 black Americans with hypertensive renal disease participating in the African American Study of Kidney Disease (AASK).]. 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:18385420;
    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:NP343908.RA5QHWkWTXVGIXXH6RGCo0PMIcjglKLQdnB0HwbYd4Xb8130_publicationInfo {
  this: dcterms:created "2015-08-25T14:40:58+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" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}