@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP846596.RAhYAMAiHEmkyk5L4MB1otuyK3B1GysWDOUKIDwBa1Gqo
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP846596.RAhYAMAiHEmkyk5L4MB1otuyK3B1GysWDOUKIDwBa1Gqo130_head
{
this:
np:hasAssertion
dgn-np:NP846596.RAhYAMAiHEmkyk5L4MB1otuyK3B1GysWDOUKIDwBa1Gqo130_assertion
;
np:hasProvenance
dgn-np:NP846596.RAhYAMAiHEmkyk5L4MB1otuyK3B1GysWDOUKIDwBa1Gqo130_provenance
;
np:hasPublicationInfo
dgn-np:NP846596.RAhYAMAiHEmkyk5L4MB1otuyK3B1GysWDOUKIDwBa1Gqo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP846596.RAhYAMAiHEmkyk5L4MB1otuyK3B1GysWDOUKIDwBa1Gqo130_assertion
a
np:Assertion
.
dgn-np:NP846596.RAhYAMAiHEmkyk5L4MB1otuyK3B1GysWDOUKIDwBa1Gqo130_provenance
a
np:Provenance
.
dgn-np:NP846596.RAhYAMAiHEmkyk5L4MB1otuyK3B1GysWDOUKIDwBa1Gqo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP846596.RAhYAMAiHEmkyk5L4MB1otuyK3B1GysWDOUKIDwBa1Gqo130_assertion
{
miriam-gene:65266
a
ncit:C16612
.
lld:C0020438
a
ncit:C7057
.
dgn-gda:DGNc787a55814768cc5e2c8e46ef75b1315
sio:SIO_000628
miriam-gene:65266
,
lld:C0020438
;
a
sio:SIO_001121
.
}
dgn-np:NP846596.RAhYAMAiHEmkyk5L4MB1otuyK3B1GysWDOUKIDwBa1Gqo130_provenance
{
dgn-np:NP846596.RAhYAMAiHEmkyk5L4MB1otuyK3B1GysWDOUKIDwBa1Gqo130_assertion
dcterms:description
"[The rare autosomal dominant genetic disorder familial hyperkalemia and hypertension which is caused by mutations in WNK4 kinase, is characterized by childhood hyperkalemia and hypercalciuria, and appearance of hypertension in the third to fourth decade.]. 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:20956807
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP846596.RAhYAMAiHEmkyk5L4MB1otuyK3B1GysWDOUKIDwBa1Gqo130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:08+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}