@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP259510.RAQDntsbAfcLcgpp0PnfnL5D1S7N34ZlG5s1fYTphYnpQ
> .
@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:NP259510.RAQDntsbAfcLcgpp0PnfnL5D1S7N34ZlG5s1fYTphYnpQ130_head
{
this:
np:hasAssertion
dgn-np:NP259510.RAQDntsbAfcLcgpp0PnfnL5D1S7N34ZlG5s1fYTphYnpQ130_assertion
;
np:hasProvenance
dgn-np:NP259510.RAQDntsbAfcLcgpp0PnfnL5D1S7N34ZlG5s1fYTphYnpQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP259510.RAQDntsbAfcLcgpp0PnfnL5D1S7N34ZlG5s1fYTphYnpQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP259510.RAQDntsbAfcLcgpp0PnfnL5D1S7N34ZlG5s1fYTphYnpQ130_assertion
a
np:Assertion
.
dgn-np:NP259510.RAQDntsbAfcLcgpp0PnfnL5D1S7N34ZlG5s1fYTphYnpQ130_provenance
a
np:Provenance
.
dgn-np:NP259510.RAQDntsbAfcLcgpp0PnfnL5D1S7N34ZlG5s1fYTphYnpQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP259510.RAQDntsbAfcLcgpp0PnfnL5D1S7N34ZlG5s1fYTphYnpQ130_assertion
{
miriam-gene:4306
a
ncit:C16612
.
lld:C0268436
a
ncit:C7057
.
dgn-gda:DGNb9d51467ca78d465936c889c8149e595
sio:SIO_000628
miriam-gene:4306
,
lld:C0268436
;
a
sio:SIO_001121
.
}
dgn-np:NP259510.RAQDntsbAfcLcgpp0PnfnL5D1S7N34ZlG5s1fYTphYnpQ130_provenance
{
dgn-np:NP259510.RAQDntsbAfcLcgpp0PnfnL5D1S7N34ZlG5s1fYTphYnpQ130_assertion
dcterms:description
"[Loss of function defects due to mutations in the channel subunits themselves, or in the mineralocorticoid receptor (pseudohypoaldosteronism, type I) also affect blood pressure regulation consequent to renal salt wasting and dysregulation of the epithelial sodium channel in the cortical collecting tubule.]. 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:10435675
;
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:NP259510.RAQDntsbAfcLcgpp0PnfnL5D1S7N34ZlG5s1fYTphYnpQ130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:43:43+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" .
}