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http://rdf.disgenet.org/nanopublications.trig#NP659497.RAx2Nhpdb42Dp067sVv4HstyBNLFY1ibc7fExtdc8aDuQ
> .
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http://www.w3.org/2000/01/rdf-schema#
> .
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http://www.w3.org/2001/XMLSchema#
> .
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http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
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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:NP659497.RAx2Nhpdb42Dp067sVv4HstyBNLFY1ibc7fExtdc8aDuQ130_head
{
this:
np:hasAssertion
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;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP659497.RAx2Nhpdb42Dp067sVv4HstyBNLFY1ibc7fExtdc8aDuQ130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP659497.RAx2Nhpdb42Dp067sVv4HstyBNLFY1ibc7fExtdc8aDuQ130_assertion
a
np:Assertion
.
dgn-np:NP659497.RAx2Nhpdb42Dp067sVv4HstyBNLFY1ibc7fExtdc8aDuQ130_provenance
a
np:Provenance
.
dgn-np:NP659497.RAx2Nhpdb42Dp067sVv4HstyBNLFY1ibc7fExtdc8aDuQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP659497.RAx2Nhpdb42Dp067sVv4HstyBNLFY1ibc7fExtdc8aDuQ130_assertion
{
miriam-gene:65125
a
ncit:C16612
.
lld:C0220666
a
ncit:C7057
.
dgn-gda:DGN5573c3f40527c8a937d67988d85bcc14
sio:SIO_000628
miriam-gene:65125
,
lld:C0220666
;
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.
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dgn-np:NP659497.RAx2Nhpdb42Dp067sVv4HstyBNLFY1ibc7fExtdc8aDuQ130_provenance
{
dgn-np:NP659497.RAx2Nhpdb42Dp067sVv4HstyBNLFY1ibc7fExtdc8aDuQ130_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
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sio:SIO_000772
miriam-pubmed:15888480
;
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 .
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dgn-np:NP659497.RAx2Nhpdb42Dp067sVv4HstyBNLFY1ibc7fExtdc8aDuQ130_publicationInfo
{
this:
dcterms:created
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xsd:dateTime
;
dcterms:rights
<
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> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
;
prv:usedData
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> , <
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> , <
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
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