@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP909051.RAuwhGN1X9LzYslHww2CH5cf-1ckGr4unTJ15ymzqRQAc
> .
@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:NP909051.RAuwhGN1X9LzYslHww2CH5cf-1ckGr4unTJ15ymzqRQAc130_head
{
this:
np:hasAssertion
dgn-np:NP909051.RAuwhGN1X9LzYslHww2CH5cf-1ckGr4unTJ15ymzqRQAc130_assertion
;
np:hasProvenance
dgn-np:NP909051.RAuwhGN1X9LzYslHww2CH5cf-1ckGr4unTJ15ymzqRQAc130_provenance
;
np:hasPublicationInfo
dgn-np:NP909051.RAuwhGN1X9LzYslHww2CH5cf-1ckGr4unTJ15ymzqRQAc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP909051.RAuwhGN1X9LzYslHww2CH5cf-1ckGr4unTJ15ymzqRQAc130_assertion
a
np:Assertion
.
dgn-np:NP909051.RAuwhGN1X9LzYslHww2CH5cf-1ckGr4unTJ15ymzqRQAc130_provenance
a
np:Provenance
.
dgn-np:NP909051.RAuwhGN1X9LzYslHww2CH5cf-1ckGr4unTJ15ymzqRQAc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP909051.RAuwhGN1X9LzYslHww2CH5cf-1ckGr4unTJ15ymzqRQAc130_assertion
{
miriam-gene:6559
a
ncit:C16612
.
lld:C0020428
a
ncit:C7057
.
dgn-gda:DGNa7f1c12b7e4b3f95e9e5d4a3db7db10b
sio:SIO_000628
miriam-gene:6559
,
lld:C0020428
;
a
sio:SIO_001121
.
}
dgn-np:NP909051.RAuwhGN1X9LzYslHww2CH5cf-1ckGr4unTJ15ymzqRQAc130_provenance
{
dgn-np:NP909051.RAuwhGN1X9LzYslHww2CH5cf-1ckGr4unTJ15ymzqRQAc130_assertion
dcterms:description
"[The defective function of the NCCT, which normally is expressed in the apical membrane of the distal convolute tubule in the kidney, leads to mild hypotension, hypokalemia, hyperreninemic hyperaldosteronism, mild metabolic alkalosis, hypomagnesemia and hypocalciuria.]. 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:17654016
;
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 .
}
dgn-np:NP909051.RAuwhGN1X9LzYslHww2CH5cf-1ckGr4unTJ15ymzqRQAc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:18+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" .
}