@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP697849.RA1cBDGWl2TvfqBgeugpO8qJpmYPjqrHr1Sn6zY5IWlWs> .
@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 dcterms: <http://purl.org/dc/terms/> .
@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:NP697849.RA1cBDGWl2TvfqBgeugpO8qJpmYPjqrHr1Sn6zY5IWlWs130_head {
  this: np:hasAssertion dgn-np:NP697849.RA1cBDGWl2TvfqBgeugpO8qJpmYPjqrHr1Sn6zY5IWlWs130_assertion ;
    np:hasProvenance dgn-np:NP697849.RA1cBDGWl2TvfqBgeugpO8qJpmYPjqrHr1Sn6zY5IWlWs130_provenance ;
    np:hasPublicationInfo dgn-np:NP697849.RA1cBDGWl2TvfqBgeugpO8qJpmYPjqrHr1Sn6zY5IWlWs130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP697849.RA1cBDGWl2TvfqBgeugpO8qJpmYPjqrHr1Sn6zY5IWlWs130_assertion a np:Assertion .
  dgn-np:NP697849.RA1cBDGWl2TvfqBgeugpO8qJpmYPjqrHr1Sn6zY5IWlWs130_provenance a np:Provenance .
  dgn-np:NP697849.RA1cBDGWl2TvfqBgeugpO8qJpmYPjqrHr1Sn6zY5IWlWs130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP697849.RA1cBDGWl2TvfqBgeugpO8qJpmYPjqrHr1Sn6zY5IWlWs130_assertion {
  miriam-gene:3778 a ncit:C16612 .
  lld:C0038454 a ncit:C7057 .
  dgn-gda:DGNdce5608a85937f73836aa9c4d3f185e0 sio:SIO_000628 miriam-gene:3778 , lld:C0038454 ;
    a sio:SIO_001121 .
}
dgn-np:NP697849.RA1cBDGWl2TvfqBgeugpO8qJpmYPjqrHr1Sn6zY5IWlWs130_provenance {
  dgn-np:NP697849.RA1cBDGWl2TvfqBgeugpO8qJpmYPjqrHr1Sn6zY5IWlWs130_assertion dcterms:description "[Our study provides the first genetic evidence for the different impact of the BK channel in the control of human blood pressure in men and women, with particular relevance in aging women, and highlights the E65K polymorphism as one of the strongest genetic factors associated thus far to protection against myocardial infarction and stroke.]. 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:16293791 ;
    prov:wasDerivedFrom dgn-void:befree-20140225 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP697849.RA1cBDGWl2TvfqBgeugpO8qJpmYPjqrHr1Sn6zY5IWlWs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:04+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:disgenetrdf ;
    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 "v2.1.0.0" .
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}