@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP59618.RA4fpwyKYpyDJ949C8emGKqaGWgab0oH72KGGSdbZmz9w
> .
@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 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:NP59618.RA4fpwyKYpyDJ949C8emGKqaGWgab0oH72KGGSdbZmz9w130_head
{
this:
np:hasAssertion
dgn-np:NP59618.RA4fpwyKYpyDJ949C8emGKqaGWgab0oH72KGGSdbZmz9w130_assertion
;
np:hasProvenance
dgn-np:NP59618.RA4fpwyKYpyDJ949C8emGKqaGWgab0oH72KGGSdbZmz9w130_provenance
;
np:hasPublicationInfo
dgn-np:NP59618.RA4fpwyKYpyDJ949C8emGKqaGWgab0oH72KGGSdbZmz9w130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP59618.RA4fpwyKYpyDJ949C8emGKqaGWgab0oH72KGGSdbZmz9w130_assertion
a
np:Assertion
.
dgn-np:NP59618.RA4fpwyKYpyDJ949C8emGKqaGWgab0oH72KGGSdbZmz9w130_provenance
a
np:Provenance
.
dgn-np:NP59618.RA4fpwyKYpyDJ949C8emGKqaGWgab0oH72KGGSdbZmz9w130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP59618.RA4fpwyKYpyDJ949C8emGKqaGWgab0oH72KGGSdbZmz9w130_assertion
{
miriam-gene:476
a
ncit:C16612
.
lld:C0020538
a
ncit:C7057
.
dgn-gda:DGN5440061fbd3e3a3e1a8accf3fa37e18f
sio:SIO_000628
miriam-gene:476
,
lld:C0020538
;
a
sio:SIO_001122
.
}
dgn-np:NP59618.RA4fpwyKYpyDJ949C8emGKqaGWgab0oH72KGGSdbZmz9w130_provenance
{
dgn-np:NP59618.RA4fpwyKYpyDJ949C8emGKqaGWgab0oH72KGGSdbZmz9w130_assertion
dct:description
"[The data are compelling that ATP1A1 and NKCC2 genes are candidate interacting hypertension-susceptibility loci in human essential hypertension and affirm gene interaction as an important genetic mechanism underlying hypertension susceptibility. Although corroboration in other cohorts and identification of functionally significant mutations are imperative next steps, the data provide a genotype-stratification scheme, with 4-fold predictive value (odds ratio, 4.28; 95% confidence interval, 2.29 to 8.0), which could help decipher the complex genetics of essential hypertension.]. 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:11509477
;
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:NP59618.RA4fpwyKYpyDJ949C8emGKqaGWgab0oH72KGGSdbZmz9w130_publicationInfo
{
this:
dct:created
"2014-10-02T12:32:28+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}