@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP500353.RABTxGrITPh8axoXcaTj9TcSsuWxHLXs04_8-bZiuD_KU
> .
@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:NP500353.RABTxGrITPh8axoXcaTj9TcSsuWxHLXs04_8-bZiuD_KU130_head
{
this:
np:hasAssertion
dgn-np:NP500353.RABTxGrITPh8axoXcaTj9TcSsuWxHLXs04_8-bZiuD_KU130_assertion
;
np:hasProvenance
dgn-np:NP500353.RABTxGrITPh8axoXcaTj9TcSsuWxHLXs04_8-bZiuD_KU130_provenance
;
np:hasPublicationInfo
dgn-np:NP500353.RABTxGrITPh8axoXcaTj9TcSsuWxHLXs04_8-bZiuD_KU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP500353.RABTxGrITPh8axoXcaTj9TcSsuWxHLXs04_8-bZiuD_KU130_assertion
a
np:Assertion
.
dgn-np:NP500353.RABTxGrITPh8axoXcaTj9TcSsuWxHLXs04_8-bZiuD_KU130_provenance
a
np:Provenance
.
dgn-np:NP500353.RABTxGrITPh8axoXcaTj9TcSsuWxHLXs04_8-bZiuD_KU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP500353.RABTxGrITPh8axoXcaTj9TcSsuWxHLXs04_8-bZiuD_KU130_assertion
{
miriam-gene:7421
a
ncit:C16612
.
lld:C0020538
a
ncit:C7057
.
dgn-gda:DGNdb951f36fe2dfb03537b770a907a4f81
sio:SIO_000628
miriam-gene:7421
,
lld:C0020538
;
a
sio:SIO_001121
.
}
dgn-np:NP500353.RABTxGrITPh8axoXcaTj9TcSsuWxHLXs04_8-bZiuD_KU130_provenance
{
dgn-np:NP500353.RABTxGrITPh8axoXcaTj9TcSsuWxHLXs04_8-bZiuD_KU130_assertion
dcterms:description
"[The observation that mice with genetic disruption of the 1α-hydroxylase gene or of the VDR gene have an overstimulated RAS and consequently develop high blood pressure and cardiac hypertrophy raised concern about potential risks to the cardiovascular system in HVDRR patients.]. 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:23128575
;
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:NP500353.RABTxGrITPh8axoXcaTj9TcSsuWxHLXs04_8-bZiuD_KU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:58+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" .
}