@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP898087.RAfIA6VYdckV8er3fgwn-VpVCJchQwQTQ9Ajn6WRSYWog
> .
@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:NP898087.RAfIA6VYdckV8er3fgwn-VpVCJchQwQTQ9Ajn6WRSYWog130_head
{
this:
np:hasAssertion
dgn-np:NP898087.RAfIA6VYdckV8er3fgwn-VpVCJchQwQTQ9Ajn6WRSYWog130_assertion
;
np:hasProvenance
dgn-np:NP898087.RAfIA6VYdckV8er3fgwn-VpVCJchQwQTQ9Ajn6WRSYWog130_provenance
;
np:hasPublicationInfo
dgn-np:NP898087.RAfIA6VYdckV8er3fgwn-VpVCJchQwQTQ9Ajn6WRSYWog130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP898087.RAfIA6VYdckV8er3fgwn-VpVCJchQwQTQ9Ajn6WRSYWog130_assertion
a
np:Assertion
.
dgn-np:NP898087.RAfIA6VYdckV8er3fgwn-VpVCJchQwQTQ9Ajn6WRSYWog130_provenance
a
np:Provenance
.
dgn-np:NP898087.RAfIA6VYdckV8er3fgwn-VpVCJchQwQTQ9Ajn6WRSYWog130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP898087.RAfIA6VYdckV8er3fgwn-VpVCJchQwQTQ9Ajn6WRSYWog130_assertion
{
miriam-gene:6283
a
ncit:C16612
.
lld:C0085580
a
ncit:C7057
.
dgn-gda:DGN5932dea46bbcc69b57fd1943bf7365f2
sio:SIO_000628
miriam-gene:6283
,
lld:C0085580
;
a
sio:SIO_001121
.
}
dgn-np:NP898087.RAfIA6VYdckV8er3fgwn-VpVCJchQwQTQ9Ajn6WRSYWog130_provenance
{
dgn-np:NP898087.RAfIA6VYdckV8er3fgwn-VpVCJchQwQTQ9Ajn6WRSYWog130_assertion
dcterms:description
"[Decreased plasma CGRP level in patients with essential hypertension or SHRs is likely due to the reduced AEA transporter activity, and the increased ADMA level may account for the reduced AEA transporter activity.]. 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:19462497
;
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:NP898087.RAfIA6VYdckV8er3fgwn-VpVCJchQwQTQ9Ajn6WRSYWog130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:12+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" .
}