@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP359297.RAmgYbKjwi_z--L72eiSA50DR5VV1jij3NOGtmdYxnW7w
> .
@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:NP359297.RAmgYbKjwi_z--L72eiSA50DR5VV1jij3NOGtmdYxnW7w130_head
{
this:
np:hasAssertion
dgn-np:NP359297.RAmgYbKjwi_z--L72eiSA50DR5VV1jij3NOGtmdYxnW7w130_assertion
;
np:hasProvenance
dgn-np:NP359297.RAmgYbKjwi_z--L72eiSA50DR5VV1jij3NOGtmdYxnW7w130_provenance
;
np:hasPublicationInfo
dgn-np:NP359297.RAmgYbKjwi_z--L72eiSA50DR5VV1jij3NOGtmdYxnW7w130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP359297.RAmgYbKjwi_z--L72eiSA50DR5VV1jij3NOGtmdYxnW7w130_assertion
a
np:Assertion
.
dgn-np:NP359297.RAmgYbKjwi_z--L72eiSA50DR5VV1jij3NOGtmdYxnW7w130_provenance
a
np:Provenance
.
dgn-np:NP359297.RAmgYbKjwi_z--L72eiSA50DR5VV1jij3NOGtmdYxnW7w130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP359297.RAmgYbKjwi_z--L72eiSA50DR5VV1jij3NOGtmdYxnW7w130_assertion
{
miriam-gene:845
a
ncit:C16612
.
lld:C0018802
a
ncit:C7057
.
dgn-gda:DGN279f440993e28721a0576cb930e1f652
sio:SIO_000628
miriam-gene:845
,
lld:C0018802
;
a
sio:SIO_001121
.
}
dgn-np:NP359297.RAmgYbKjwi_z--L72eiSA50DR5VV1jij3NOGtmdYxnW7w130_provenance
{
dgn-np:NP359297.RAmgYbKjwi_z--L72eiSA50DR5VV1jij3NOGtmdYxnW7w130_assertion
dcterms:description
"[Studies on the consequences of RyR2 and CASQ2 mutations in cellular systems and mouse models have shed new light on pathways that are also implicated in arrhythmias occurring in highly prevalent diseases, such as heart failure.]. 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:19879546
;
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:NP359297.RAmgYbKjwi_z--L72eiSA50DR5VV1jij3NOGtmdYxnW7w130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:30+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" .
}