@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP532076.RAN08hvEnSDdEKH_9hioUYGjVyWoQu7M4TZbV78GhuSlg
> .
@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:NP532076.RAN08hvEnSDdEKH_9hioUYGjVyWoQu7M4TZbV78GhuSlg130_head
{
this:
np:hasAssertion
dgn-np:NP532076.RAN08hvEnSDdEKH_9hioUYGjVyWoQu7M4TZbV78GhuSlg130_assertion
;
np:hasProvenance
dgn-np:NP532076.RAN08hvEnSDdEKH_9hioUYGjVyWoQu7M4TZbV78GhuSlg130_provenance
;
np:hasPublicationInfo
dgn-np:NP532076.RAN08hvEnSDdEKH_9hioUYGjVyWoQu7M4TZbV78GhuSlg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP532076.RAN08hvEnSDdEKH_9hioUYGjVyWoQu7M4TZbV78GhuSlg130_assertion
a
np:Assertion
.
dgn-np:NP532076.RAN08hvEnSDdEKH_9hioUYGjVyWoQu7M4TZbV78GhuSlg130_provenance
a
np:Provenance
.
dgn-np:NP532076.RAN08hvEnSDdEKH_9hioUYGjVyWoQu7M4TZbV78GhuSlg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP532076.RAN08hvEnSDdEKH_9hioUYGjVyWoQu7M4TZbV78GhuSlg130_assertion
{
miriam-gene:156
a
ncit:C16612
.
lld:C0018802
a
ncit:C7057
.
dgn-gda:DGN19e4cad9d5c31b356228f63826192f40
sio:SIO_000628
miriam-gene:156
,
lld:C0018802
;
a
sio:SIO_001121
.
}
dgn-np:NP532076.RAN08hvEnSDdEKH_9hioUYGjVyWoQu7M4TZbV78GhuSlg130_provenance
{
dgn-np:NP532076.RAN08hvEnSDdEKH_9hioUYGjVyWoQu7M4TZbV78GhuSlg130_assertion
dcterms:description
"[The present review gives first a brief account of what has already been documented about the benefits of cardiac GRK2 genetic manipulation in HF as a positive inotropic therapy for the disease, and then goes on to discuss in detail the intriguing new possibility that has emerged of lowering GRK2 activity in the adrenal gland, which could constitute a novel sympatholytic therapy for HF that helps relieve the devastatingly cardiotoxic sympathetic overload of the failing heart.]. 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:22229578
;
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:NP532076.RAN08hvEnSDdEKH_9hioUYGjVyWoQu7M4TZbV78GhuSlg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:21+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" .
}