@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP219035.RAk5Q9Y8Qemsj4NdufAqQDAKMPz43L6SzufTSX2rJKhVg
> .
@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:NP219035.RAk5Q9Y8Qemsj4NdufAqQDAKMPz43L6SzufTSX2rJKhVg130_head
{
this:
np:hasAssertion
dgn-np:NP219035.RAk5Q9Y8Qemsj4NdufAqQDAKMPz43L6SzufTSX2rJKhVg130_assertion
;
np:hasProvenance
dgn-np:NP219035.RAk5Q9Y8Qemsj4NdufAqQDAKMPz43L6SzufTSX2rJKhVg130_provenance
;
np:hasPublicationInfo
dgn-np:NP219035.RAk5Q9Y8Qemsj4NdufAqQDAKMPz43L6SzufTSX2rJKhVg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP219035.RAk5Q9Y8Qemsj4NdufAqQDAKMPz43L6SzufTSX2rJKhVg130_assertion
a
np:Assertion
.
dgn-np:NP219035.RAk5Q9Y8Qemsj4NdufAqQDAKMPz43L6SzufTSX2rJKhVg130_provenance
a
np:Provenance
.
dgn-np:NP219035.RAk5Q9Y8Qemsj4NdufAqQDAKMPz43L6SzufTSX2rJKhVg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP219035.RAk5Q9Y8Qemsj4NdufAqQDAKMPz43L6SzufTSX2rJKhVg130_assertion
{
miriam-gene:6559
a
ncit:C16612
.
lld:C0020538
a
ncit:C7057
.
dgn-gda:DGN41f85a0ffe9226729a355202dbac6c31
sio:SIO_000628
miriam-gene:6559
,
lld:C0020538
;
a
sio:SIO_001121
.
}
dgn-np:NP219035.RAk5Q9Y8Qemsj4NdufAqQDAKMPz43L6SzufTSX2rJKhVg130_provenance
{
dgn-np:NP219035.RAk5Q9Y8Qemsj4NdufAqQDAKMPz43L6SzufTSX2rJKhVg130_assertion
dcterms:description
"[The increased urinary NCCT in FHH most probably reflects increased NCCT abundance in the apical membrane of distal tubule cells in patients with FHH and the WNK4 mutation and points to the pathogenetic mechanism for the clinical phenotype of FHH and the WNK4 mutation, supporting results in transgenic mice with the same mutation and in knockin mice with another mutation.]. 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:17951312
;
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:NP219035.RAk5Q9Y8Qemsj4NdufAqQDAKMPz43L6SzufTSX2rJKhVg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:01+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" .
}