@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1354533.RA-HuoLt_-uQECkGv0hhM3hYRtu_4Iz8OhAIs4uuVx6a8
> .
@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:NP1354533.RA-HuoLt_-uQECkGv0hhM3hYRtu_4Iz8OhAIs4uuVx6a8130_head
{
this:
np:hasAssertion
dgn-np:NP1354533.RA-HuoLt_-uQECkGv0hhM3hYRtu_4Iz8OhAIs4uuVx6a8130_assertion
;
np:hasProvenance
dgn-np:NP1354533.RA-HuoLt_-uQECkGv0hhM3hYRtu_4Iz8OhAIs4uuVx6a8130_provenance
;
np:hasPublicationInfo
dgn-np:NP1354533.RA-HuoLt_-uQECkGv0hhM3hYRtu_4Iz8OhAIs4uuVx6a8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1354533.RA-HuoLt_-uQECkGv0hhM3hYRtu_4Iz8OhAIs4uuVx6a8130_assertion
a
np:Assertion
.
dgn-np:NP1354533.RA-HuoLt_-uQECkGv0hhM3hYRtu_4Iz8OhAIs4uuVx6a8130_provenance
a
np:Provenance
.
dgn-np:NP1354533.RA-HuoLt_-uQECkGv0hhM3hYRtu_4Iz8OhAIs4uuVx6a8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1354533.RA-HuoLt_-uQECkGv0hhM3hYRtu_4Iz8OhAIs4uuVx6a8130_assertion
{
miriam-gene:5972
a
ncit:C16612
.
lld:C0020538
a
ncit:C7057
.
dgn-gda:DGNb3d46766a5e43be4fc28927f5d2d007d
sio:SIO_000628
miriam-gene:5972
,
lld:C0020538
;
a
sio:SIO_001121
.
}
dgn-np:NP1354533.RA-HuoLt_-uQECkGv0hhM3hYRtu_4Iz8OhAIs4uuVx6a8130_provenance
{
dgn-np:NP1354533.RA-HuoLt_-uQECkGv0hhM3hYRtu_4Iz8OhAIs4uuVx6a8130_assertion
dcterms:description
"[The syndrome of apparent mineralocorticoid excess (AME) is a heritable form of hypertension due to an inborn error of cortisol metabolism and is characterized by hypokalemia and low renin levels despite subnormal or normal levels of aldosterone and other known mineralocorticoids.]. 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:8732999
;
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:NP1354533.RA-HuoLt_-uQECkGv0hhM3hYRtu_4Iz8OhAIs4uuVx6a8130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:52:00+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" .
}