@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP311869.RAWzayHIMTmFL042k9-2ZAjs3wz0i1eQ2BcqLRnqKlHU8
> .
@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:NP311869.RAWzayHIMTmFL042k9-2ZAjs3wz0i1eQ2BcqLRnqKlHU8130_head
{
this:
np:hasAssertion
dgn-np:NP311869.RAWzayHIMTmFL042k9-2ZAjs3wz0i1eQ2BcqLRnqKlHU8130_assertion
;
np:hasProvenance
dgn-np:NP311869.RAWzayHIMTmFL042k9-2ZAjs3wz0i1eQ2BcqLRnqKlHU8130_provenance
;
np:hasPublicationInfo
dgn-np:NP311869.RAWzayHIMTmFL042k9-2ZAjs3wz0i1eQ2BcqLRnqKlHU8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP311869.RAWzayHIMTmFL042k9-2ZAjs3wz0i1eQ2BcqLRnqKlHU8130_assertion
a
np:Assertion
.
dgn-np:NP311869.RAWzayHIMTmFL042k9-2ZAjs3wz0i1eQ2BcqLRnqKlHU8130_provenance
a
np:Provenance
.
dgn-np:NP311869.RAWzayHIMTmFL042k9-2ZAjs3wz0i1eQ2BcqLRnqKlHU8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP311869.RAWzayHIMTmFL042k9-2ZAjs3wz0i1eQ2BcqLRnqKlHU8130_assertion
{
miriam-gene:1585
a
ncit:C16612
.
lld:C0020428
a
ncit:C7057
.
dgn-gda:DGN120a18e7253f85fd168f482d2c764ac8
sio:SIO_000628
miriam-gene:1585
,
lld:C0020428
;
a
sio:SIO_001121
.
}
dgn-np:NP311869.RAWzayHIMTmFL042k9-2ZAjs3wz0i1eQ2BcqLRnqKlHU8130_provenance
{
dgn-np:NP311869.RAWzayHIMTmFL042k9-2ZAjs3wz0i1eQ2BcqLRnqKlHU8130_assertion
dcterms:description
"[There is recent evidence suggesting that hyperaldosteronism relates to aldosterone synthase genetic polymorphism, and also that increased angiotensin II stimulation of the adrenal glands appears to paradoxically upregulate the receptors increasing angiotensin II sensitivity.]. 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:11791020
;
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:NP311869.RAWzayHIMTmFL042k9-2ZAjs3wz0i1eQ2BcqLRnqKlHU8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:59+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" .
}