@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP800589.RA8Bv72Xr6RdYGFXAbRhosAQS5ldeSRndOjN6p-yknn8o
> .
@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:NP800589.RA8Bv72Xr6RdYGFXAbRhosAQS5ldeSRndOjN6p-yknn8o130_head
{
this:
np:hasAssertion
dgn-np:NP800589.RA8Bv72Xr6RdYGFXAbRhosAQS5ldeSRndOjN6p-yknn8o130_assertion
;
np:hasProvenance
dgn-np:NP800589.RA8Bv72Xr6RdYGFXAbRhosAQS5ldeSRndOjN6p-yknn8o130_provenance
;
np:hasPublicationInfo
dgn-np:NP800589.RA8Bv72Xr6RdYGFXAbRhosAQS5ldeSRndOjN6p-yknn8o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP800589.RA8Bv72Xr6RdYGFXAbRhosAQS5ldeSRndOjN6p-yknn8o130_assertion
a
np:Assertion
.
dgn-np:NP800589.RA8Bv72Xr6RdYGFXAbRhosAQS5ldeSRndOjN6p-yknn8o130_provenance
a
np:Provenance
.
dgn-np:NP800589.RA8Bv72Xr6RdYGFXAbRhosAQS5ldeSRndOjN6p-yknn8o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP800589.RA8Bv72Xr6RdYGFXAbRhosAQS5ldeSRndOjN6p-yknn8o130_assertion
{
miriam-gene:4306
a
ncit:C16612
.
lld:C0030779
a
ncit:C7057
.
dgn-gda:DGN5d27daadff043da43a6fda00428ca4bc
sio:SIO_000628
miriam-gene:4306
,
lld:C0030779
;
a
sio:SIO_001121
.
}
dgn-np:NP800589.RA8Bv72Xr6RdYGFXAbRhosAQS5ldeSRndOjN6p-yknn8o130_provenance
{
dgn-np:NP800589.RA8Bv72Xr6RdYGFXAbRhosAQS5ldeSRndOjN6p-yknn8o130_assertion
dcterms:description
"[Mineralocorticoid receptor (MR) and postreceptor defects in the aldosterone-responsive amiloride-sensitive sodium channel (ENaC) subunits have been suggested as potential loci of the defect in this disease, whereas recently defects in MR and ENaC subunits were reported in familial PHA cases.]. 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:10404817
;
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:NP800589.RA8Bv72Xr6RdYGFXAbRhosAQS5ldeSRndOjN6p-yknn8o130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:11+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" .
}