@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP822044.RA_3V2D1vQI-T2zX0dqoBBWnEfonX1Cf6nDDHwi_PRw-Q
> .
@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:NP822044.RA_3V2D1vQI-T2zX0dqoBBWnEfonX1Cf6nDDHwi_PRw-Q130_head
{
this:
np:hasAssertion
dgn-np:NP822044.RA_3V2D1vQI-T2zX0dqoBBWnEfonX1Cf6nDDHwi_PRw-Q130_assertion
;
np:hasProvenance
dgn-np:NP822044.RA_3V2D1vQI-T2zX0dqoBBWnEfonX1Cf6nDDHwi_PRw-Q130_provenance
;
np:hasPublicationInfo
dgn-np:NP822044.RA_3V2D1vQI-T2zX0dqoBBWnEfonX1Cf6nDDHwi_PRw-Q130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP822044.RA_3V2D1vQI-T2zX0dqoBBWnEfonX1Cf6nDDHwi_PRw-Q130_assertion
a
np:Assertion
.
dgn-np:NP822044.RA_3V2D1vQI-T2zX0dqoBBWnEfonX1Cf6nDDHwi_PRw-Q130_provenance
a
np:Provenance
.
dgn-np:NP822044.RA_3V2D1vQI-T2zX0dqoBBWnEfonX1Cf6nDDHwi_PRw-Q130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP822044.RA_3V2D1vQI-T2zX0dqoBBWnEfonX1Cf6nDDHwi_PRw-Q130_assertion
{
miriam-gene:6559
a
ncit:C16612
.
lld:C1449844
a
ncit:C7057
.
dgn-gda:DGN17336adc4acb6b4d6675221869d517fc
sio:SIO_000628
miriam-gene:6559
,
lld:C1449844
;
a
sio:SIO_001121
.
}
dgn-np:NP822044.RA_3V2D1vQI-T2zX0dqoBBWnEfonX1Cf6nDDHwi_PRw-Q130_provenance
{
dgn-np:NP822044.RA_3V2D1vQI-T2zX0dqoBBWnEfonX1Cf6nDDHwi_PRw-Q130_assertion
dcterms:description
"[It has been appreciated for several years that WNK kinases affect NCC expression, following the discovery that mutations in WNK genes cause Gordon syndrome (pseudohypoaldosteronism type II), although the precise molecular mechanisms were unclear.]. 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:21088576
;
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:NP822044.RA_3V2D1vQI-T2zX0dqoBBWnEfonX1Cf6nDDHwi_PRw-Q130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:23+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" .
}