@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP566003.RAvFqzitAbvtO7_1UHmp5vPz8Kg2Vi2LmZi9trgk3gp4g
> .
@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:NP566003.RAvFqzitAbvtO7_1UHmp5vPz8Kg2Vi2LmZi9trgk3gp4g130_head
{
this:
np:hasAssertion
dgn-np:NP566003.RAvFqzitAbvtO7_1UHmp5vPz8Kg2Vi2LmZi9trgk3gp4g130_assertion
;
np:hasProvenance
dgn-np:NP566003.RAvFqzitAbvtO7_1UHmp5vPz8Kg2Vi2LmZi9trgk3gp4g130_provenance
;
np:hasPublicationInfo
dgn-np:NP566003.RAvFqzitAbvtO7_1UHmp5vPz8Kg2Vi2LmZi9trgk3gp4g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP566003.RAvFqzitAbvtO7_1UHmp5vPz8Kg2Vi2LmZi9trgk3gp4g130_assertion
a
np:Assertion
.
dgn-np:NP566003.RAvFqzitAbvtO7_1UHmp5vPz8Kg2Vi2LmZi9trgk3gp4g130_provenance
a
np:Provenance
.
dgn-np:NP566003.RAvFqzitAbvtO7_1UHmp5vPz8Kg2Vi2LmZi9trgk3gp4g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP566003.RAvFqzitAbvtO7_1UHmp5vPz8Kg2Vi2LmZi9trgk3gp4g130_assertion
{
miriam-gene:472
a
ncit:C16612
.
lld:C0020538
a
ncit:C7057
.
dgn-gda:DGNc09f62fc42da8fd9289339154278d532
sio:SIO_000628
miriam-gene:472
,
lld:C0020538
;
a
sio:SIO_001121
.
}
dgn-np:NP566003.RAvFqzitAbvtO7_1UHmp5vPz8Kg2Vi2LmZi9trgk3gp4g130_provenance
{
dgn-np:NP566003.RAvFqzitAbvtO7_1UHmp5vPz8Kg2Vi2LmZi9trgk3gp4g130_assertion
dcterms:description
"[The aim of this study was to assess the relationship between the A1166C polymorphism of the angiotensin AT1 receptor gene and reduction of blood pressure and pulse pressure in patients with mild and moderate arterial hypertension.]. 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:18575418
;
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:NP566003.RAvFqzitAbvtO7_1UHmp5vPz8Kg2Vi2LmZi9trgk3gp4g130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:41+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" .
}