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http://rdf.disgenet.org/nanopublications.trig#NP59287.RAsGMKg-RYUeabzaKGhhu_-wPVMkAtBgISZb_nMUqBRug
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP59287.RAsGMKg-RYUeabzaKGhhu_-wPVMkAtBgISZb_nMUqBRug130_assertion
;
np:hasProvenance
dgn-np:NP59287.RAsGMKg-RYUeabzaKGhhu_-wPVMkAtBgISZb_nMUqBRug130_provenance
;
np:hasPublicationInfo
dgn-np:NP59287.RAsGMKg-RYUeabzaKGhhu_-wPVMkAtBgISZb_nMUqBRug130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP59287.RAsGMKg-RYUeabzaKGhhu_-wPVMkAtBgISZb_nMUqBRug130_assertion
a
np:Assertion
.
dgn-np:NP59287.RAsGMKg-RYUeabzaKGhhu_-wPVMkAtBgISZb_nMUqBRug130_provenance
a
np:Provenance
.
dgn-np:NP59287.RAsGMKg-RYUeabzaKGhhu_-wPVMkAtBgISZb_nMUqBRug130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP59287.RAsGMKg-RYUeabzaKGhhu_-wPVMkAtBgISZb_nMUqBRug130_assertion
{
miriam-gene:65266
a
ncit:C16612
.
lld:C0020538
a
ncit:C7057
.
dgn-gda:DGN5d1b1690574ca2ece144199b91f8999e
sio:SIO_000628
miriam-gene:65266
,
lld:C0020538
;
a
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.
}
dgn-np:NP59287.RAsGMKg-RYUeabzaKGhhu_-wPVMkAtBgISZb_nMUqBRug130_provenance
{
dgn-np:NP59287.RAsGMKg-RYUeabzaKGhhu_-wPVMkAtBgISZb_nMUqBRug130_assertion
dcterms:description
"[No significant differences in allelic or genotypic frequencies were observed in African Americans for any SNPs. The finding in whites is consistent with the hypothesis that polymorphisms in WNK4 influence the risk of hypertension. However, because the associated SNP does not appear to be a functional variant and the limitations of case/control association studies, confirmation of these results in additional cohorts is warranted.]. 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:12719438
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP59287.RAsGMKg-RYUeabzaKGhhu_-wPVMkAtBgISZb_nMUqBRug130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:28+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
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;
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> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
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> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v2.1.0.0" .
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"v2.1.0" .
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