@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP52094.RAroeGnWbtla8Laxv0_93NdYPAJYKEgyaiuFpfELT2LLg
> .
@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:NP52094.RAroeGnWbtla8Laxv0_93NdYPAJYKEgyaiuFpfELT2LLg130_head
{
this:
np:hasAssertion
dgn-np:NP52094.RAroeGnWbtla8Laxv0_93NdYPAJYKEgyaiuFpfELT2LLg130_assertion
;
np:hasProvenance
dgn-np:NP52094.RAroeGnWbtla8Laxv0_93NdYPAJYKEgyaiuFpfELT2LLg130_provenance
;
np:hasPublicationInfo
dgn-np:NP52094.RAroeGnWbtla8Laxv0_93NdYPAJYKEgyaiuFpfELT2LLg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP52094.RAroeGnWbtla8Laxv0_93NdYPAJYKEgyaiuFpfELT2LLg130_assertion
a
np:Assertion
.
dgn-np:NP52094.RAroeGnWbtla8Laxv0_93NdYPAJYKEgyaiuFpfELT2LLg130_provenance
a
np:Provenance
.
dgn-np:NP52094.RAroeGnWbtla8Laxv0_93NdYPAJYKEgyaiuFpfELT2LLg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP52094.RAroeGnWbtla8Laxv0_93NdYPAJYKEgyaiuFpfELT2LLg130_assertion
{
miriam-gene:6338
a
ncit:C16612
.
lld:C0020538
a
ncit:C7057
.
dgn-gda:DGN6c4df38e238b768f0b135badebf0ad51
sio:SIO_000628
miriam-gene:6338
,
lld:C0020538
;
a
sio:SIO_001122
.
}
dgn-np:NP52094.RAroeGnWbtla8Laxv0_93NdYPAJYKEgyaiuFpfELT2LLg130_provenance
{
dgn-np:NP52094.RAroeGnWbtla8Laxv0_93NdYPAJYKEgyaiuFpfELT2LLg130_assertion
dcterms:description
"[ At least 9% of Finnish patients with hypertension admitted to a specialized center carry genetic variants of beta and gammaENaC, a three times higher prevalence than in the normotensive individuals or in random healthy controls. Patients with the variant alleles showed an increased urinary potassium excretion rate in relation to their renin levels.]. 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:15661075
;
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:NP52094.RAroeGnWbtla8Laxv0_93NdYPAJYKEgyaiuFpfELT2LLg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:24+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" .
}