@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP941281.RAZlH5oPwQWxudj9RYxaCdakLDDBYHUBbIJhSdFmQXWck
> .
@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:NP941281.RAZlH5oPwQWxudj9RYxaCdakLDDBYHUBbIJhSdFmQXWck130_head
{
this:
np:hasAssertion
dgn-np:NP941281.RAZlH5oPwQWxudj9RYxaCdakLDDBYHUBbIJhSdFmQXWck130_assertion
;
np:hasProvenance
dgn-np:NP941281.RAZlH5oPwQWxudj9RYxaCdakLDDBYHUBbIJhSdFmQXWck130_provenance
;
np:hasPublicationInfo
dgn-np:NP941281.RAZlH5oPwQWxudj9RYxaCdakLDDBYHUBbIJhSdFmQXWck130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP941281.RAZlH5oPwQWxudj9RYxaCdakLDDBYHUBbIJhSdFmQXWck130_assertion
a
np:Assertion
.
dgn-np:NP941281.RAZlH5oPwQWxudj9RYxaCdakLDDBYHUBbIJhSdFmQXWck130_provenance
a
np:Provenance
.
dgn-np:NP941281.RAZlH5oPwQWxudj9RYxaCdakLDDBYHUBbIJhSdFmQXWck130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP941281.RAZlH5oPwQWxudj9RYxaCdakLDDBYHUBbIJhSdFmQXWck130_assertion
{
miriam-gene:65125
a
ncit:C16612
.
lld:C0085580
a
ncit:C7057
.
dgn-gda:DGNb6d5de4f96f58525015a7ad44d76872f
sio:SIO_000628
miriam-gene:65125
,
lld:C0085580
;
a
sio:SIO_001121
.
}
dgn-np:NP941281.RAZlH5oPwQWxudj9RYxaCdakLDDBYHUBbIJhSdFmQXWck130_provenance
{
dgn-np:NP941281.RAZlH5oPwQWxudj9RYxaCdakLDDBYHUBbIJhSdFmQXWck130_assertion
dcterms:description
"[This finding of association between a SNP near the promoter region and the severity of hypertension suggests that increased expression of WNK1 might contribute to BP variability and susceptibility to EH similar to the mechanism of hypertension observed in Gordon's syndrome.]. 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:15888480
;
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:NP941281.RAZlH5oPwQWxudj9RYxaCdakLDDBYHUBbIJhSdFmQXWck130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:47:15+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" .
}