@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" .
}