@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP286467.RAv4cUxcbljIId6QTOR_s0y0LDCONqepcpNeXB2K86Qco
> .
@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:NP286467.RAv4cUxcbljIId6QTOR_s0y0LDCONqepcpNeXB2K86Qco130_head
{
this:
np:hasAssertion
dgn-np:NP286467.RAv4cUxcbljIId6QTOR_s0y0LDCONqepcpNeXB2K86Qco130_assertion
;
np:hasProvenance
dgn-np:NP286467.RAv4cUxcbljIId6QTOR_s0y0LDCONqepcpNeXB2K86Qco130_provenance
;
np:hasPublicationInfo
dgn-np:NP286467.RAv4cUxcbljIId6QTOR_s0y0LDCONqepcpNeXB2K86Qco130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP286467.RAv4cUxcbljIId6QTOR_s0y0LDCONqepcpNeXB2K86Qco130_assertion
a
np:Assertion
.
dgn-np:NP286467.RAv4cUxcbljIId6QTOR_s0y0LDCONqepcpNeXB2K86Qco130_provenance
a
np:Provenance
.
dgn-np:NP286467.RAv4cUxcbljIId6QTOR_s0y0LDCONqepcpNeXB2K86Qco130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP286467.RAv4cUxcbljIId6QTOR_s0y0LDCONqepcpNeXB2K86Qco130_assertion
{
miriam-gene:183
a
ncit:C16612
.
lld:C0018801
a
ncit:C7057
.
dgn-gda:DGN5b6ca5d5bb08caa4b38c40c247348da6
sio:SIO_000628
miriam-gene:183
,
lld:C0018801
;
a
sio:SIO_001121
.
}
dgn-np:NP286467.RAv4cUxcbljIId6QTOR_s0y0LDCONqepcpNeXB2K86Qco130_provenance
{
dgn-np:NP286467.RAv4cUxcbljIId6QTOR_s0y0LDCONqepcpNeXB2K86Qco130_assertion
dcterms:description
"[Our results show that angiotensin II and hypoxia, signals common to HF, result in increased LUC7L3 and RBM25 splicing regulators, increased binding of RBM25 to SCN5A mRNA, increased SCN5A splice variant abundances, decreased full-length SCN5A mRNA and protein, and decreased Na(+) current.]. 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:22939879
;
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:NP286467.RAv4cUxcbljIId6QTOR_s0y0LDCONqepcpNeXB2K86Qco130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:41+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" .
}