@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP908106.RAyYNEqreY8i0tv5TBib3kmfPE2YewQ2OlJh1LYbPB6I4
> .
@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:NP908106.RAyYNEqreY8i0tv5TBib3kmfPE2YewQ2OlJh1LYbPB6I4130_head
{
this:
np:hasAssertion
dgn-np:NP908106.RAyYNEqreY8i0tv5TBib3kmfPE2YewQ2OlJh1LYbPB6I4130_assertion
;
np:hasProvenance
dgn-np:NP908106.RAyYNEqreY8i0tv5TBib3kmfPE2YewQ2OlJh1LYbPB6I4130_provenance
;
np:hasPublicationInfo
dgn-np:NP908106.RAyYNEqreY8i0tv5TBib3kmfPE2YewQ2OlJh1LYbPB6I4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP908106.RAyYNEqreY8i0tv5TBib3kmfPE2YewQ2OlJh1LYbPB6I4130_assertion
a
np:Assertion
.
dgn-np:NP908106.RAyYNEqreY8i0tv5TBib3kmfPE2YewQ2OlJh1LYbPB6I4130_provenance
a
np:Provenance
.
dgn-np:NP908106.RAyYNEqreY8i0tv5TBib3kmfPE2YewQ2OlJh1LYbPB6I4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP908106.RAyYNEqreY8i0tv5TBib3kmfPE2YewQ2OlJh1LYbPB6I4130_assertion
{
miriam-gene:2028
a
ncit:C16612
.
lld:C1720983
a
ncit:C7057
.
dgn-gda:DGNcc6856b450459036210b0d5e4e2ad5bd
sio:SIO_000628
miriam-gene:2028
,
lld:C1720983
;
a
sio:SIO_001121
.
}
dgn-np:NP908106.RAyYNEqreY8i0tv5TBib3kmfPE2YewQ2OlJh1LYbPB6I4130_provenance
{
dgn-np:NP908106.RAyYNEqreY8i0tv5TBib3kmfPE2YewQ2OlJh1LYbPB6I4130_assertion
dcterms:description
"[The regulation of aldosterone secretion is exerted to a significant degree by activation of membrane K(+) and calcium channels or pumps, so it is not surprising that the known causes of disorders of aldosterone secretion in APA have been channelopathies, which activate mechanisms that increase aldosterone synthesis.]. 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:24248457
;
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:NP908106.RAyYNEqreY8i0tv5TBib3kmfPE2YewQ2OlJh1LYbPB6I4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:17+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" .
}