@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP647007.RAyTVSbh-wvC9NY0IR3ozaau1ZhFgdwPLnIZcl09vNiN4
> .
@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:NP647007.RAyTVSbh-wvC9NY0IR3ozaau1ZhFgdwPLnIZcl09vNiN4130_head
{
this:
np:hasAssertion
dgn-np:NP647007.RAyTVSbh-wvC9NY0IR3ozaau1ZhFgdwPLnIZcl09vNiN4130_assertion
;
np:hasProvenance
dgn-np:NP647007.RAyTVSbh-wvC9NY0IR3ozaau1ZhFgdwPLnIZcl09vNiN4130_provenance
;
np:hasPublicationInfo
dgn-np:NP647007.RAyTVSbh-wvC9NY0IR3ozaau1ZhFgdwPLnIZcl09vNiN4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP647007.RAyTVSbh-wvC9NY0IR3ozaau1ZhFgdwPLnIZcl09vNiN4130_assertion
a
np:Assertion
.
dgn-np:NP647007.RAyTVSbh-wvC9NY0IR3ozaau1ZhFgdwPLnIZcl09vNiN4130_provenance
a
np:Provenance
.
dgn-np:NP647007.RAyTVSbh-wvC9NY0IR3ozaau1ZhFgdwPLnIZcl09vNiN4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP647007.RAyTVSbh-wvC9NY0IR3ozaau1ZhFgdwPLnIZcl09vNiN4130_assertion
{
miriam-gene:5972
a
ncit:C16612
.
lld:C0002063
a
ncit:C7057
.
dgn-gda:DGNf04829212b0c9fb83f7edc0bb15db406
sio:SIO_000628
miriam-gene:5972
,
lld:C0002063
;
a
sio:SIO_001121
.
}
dgn-np:NP647007.RAyTVSbh-wvC9NY0IR3ozaau1ZhFgdwPLnIZcl09vNiN4130_provenance
{
dgn-np:NP647007.RAyTVSbh-wvC9NY0IR3ozaau1ZhFgdwPLnIZcl09vNiN4130_assertion
dcterms:description
"[Monogenic mutations leading to excessive activation of the mineralocorticoid pathway result, almost always, in suppressed renin and hypertension in adult life and sometimes in hypokalaemia and alkalosis, which can be severe.]. 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:16980202
;
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:NP647007.RAyTVSbh-wvC9NY0IR3ozaau1ZhFgdwPLnIZcl09vNiN4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:30+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" .
}