@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP422564.RAzhhx2q8dCtxQtPzuDVy7QQ7FK_Bq_Ivkt5iU-aG-hns
> .
@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:NP422564.RAzhhx2q8dCtxQtPzuDVy7QQ7FK_Bq_Ivkt5iU-aG-hns130_head
{
this:
np:hasAssertion
dgn-np:NP422564.RAzhhx2q8dCtxQtPzuDVy7QQ7FK_Bq_Ivkt5iU-aG-hns130_assertion
;
np:hasProvenance
dgn-np:NP422564.RAzhhx2q8dCtxQtPzuDVy7QQ7FK_Bq_Ivkt5iU-aG-hns130_provenance
;
np:hasPublicationInfo
dgn-np:NP422564.RAzhhx2q8dCtxQtPzuDVy7QQ7FK_Bq_Ivkt5iU-aG-hns130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP422564.RAzhhx2q8dCtxQtPzuDVy7QQ7FK_Bq_Ivkt5iU-aG-hns130_assertion
a
np:Assertion
.
dgn-np:NP422564.RAzhhx2q8dCtxQtPzuDVy7QQ7FK_Bq_Ivkt5iU-aG-hns130_provenance
a
np:Provenance
.
dgn-np:NP422564.RAzhhx2q8dCtxQtPzuDVy7QQ7FK_Bq_Ivkt5iU-aG-hns130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP422564.RAzhhx2q8dCtxQtPzuDVy7QQ7FK_Bq_Ivkt5iU-aG-hns130_assertion
{
miriam-gene:6012
a
ncit:C16612
.
lld:C0020538
a
ncit:C7057
.
dgn-gda:DGNfae9ba51a7a75fc86b4fc50045064172
sio:SIO_000628
miriam-gene:6012
,
lld:C0020538
;
a
sio:SIO_001121
.
}
dgn-np:NP422564.RAzhhx2q8dCtxQtPzuDVy7QQ7FK_Bq_Ivkt5iU-aG-hns130_provenance
{
dgn-np:NP422564.RAzhhx2q8dCtxQtPzuDVy7QQ7FK_Bq_Ivkt5iU-aG-hns130_assertion
dcterms:description
"[These results establish that abnormally prolonged signaling by G protein-coupled vasoconstrictor receptors can contribute to the onset of hypertension, and they suggest that genetic defects affecting the function or expression of RGS2 may be novel risk factors for development of hypertension in humans.]. 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:12588882
;
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:NP422564.RAzhhx2q8dCtxQtPzuDVy7QQ7FK_Bq_Ivkt5iU-aG-hns130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:10+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" .
}