@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP502640.RA8hSHMVEg-WUmAwPbbH0mQJdiGCMKWc2CEuB2pYCUPdM
> .
@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:NP502640.RA8hSHMVEg-WUmAwPbbH0mQJdiGCMKWc2CEuB2pYCUPdM130_head
{
this:
np:hasAssertion
dgn-np:NP502640.RA8hSHMVEg-WUmAwPbbH0mQJdiGCMKWc2CEuB2pYCUPdM130_assertion
;
np:hasProvenance
dgn-np:NP502640.RA8hSHMVEg-WUmAwPbbH0mQJdiGCMKWc2CEuB2pYCUPdM130_provenance
;
np:hasPublicationInfo
dgn-np:NP502640.RA8hSHMVEg-WUmAwPbbH0mQJdiGCMKWc2CEuB2pYCUPdM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP502640.RA8hSHMVEg-WUmAwPbbH0mQJdiGCMKWc2CEuB2pYCUPdM130_assertion
a
np:Assertion
.
dgn-np:NP502640.RA8hSHMVEg-WUmAwPbbH0mQJdiGCMKWc2CEuB2pYCUPdM130_provenance
a
np:Provenance
.
dgn-np:NP502640.RA8hSHMVEg-WUmAwPbbH0mQJdiGCMKWc2CEuB2pYCUPdM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP502640.RA8hSHMVEg-WUmAwPbbH0mQJdiGCMKWc2CEuB2pYCUPdM130_assertion
{
miriam-gene:4295
a
ncit:C16612
.
lld:C0020538
a
ncit:C7057
.
dgn-gda:DGN462f2993f2711c4bb07d450e6e531b62
sio:SIO_000628
miriam-gene:4295
,
lld:C0020538
;
a
sio:SIO_001121
.
}
dgn-np:NP502640.RA8hSHMVEg-WUmAwPbbH0mQJdiGCMKWc2CEuB2pYCUPdM130_provenance
{
dgn-np:NP502640.RA8hSHMVEg-WUmAwPbbH0mQJdiGCMKWc2CEuB2pYCUPdM130_assertion
dcterms:description
"[Six tagging SNPs and resultant haplotypes were tested for associations with hypertension risk, followed by mean arterial pressure (MAP), plasma renin activity (PRA) and the change in MAP in response to angiotensin II (AngII) infusion (AngII ΔMAP).]. 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:21490026
;
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:NP502640.RA8hSHMVEg-WUmAwPbbH0mQJdiGCMKWc2CEuB2pYCUPdM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:59+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" .
}