@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP772943.RARMzQg1X1thD5KC3IoOLAo6F-HgH-F0vQ9NY7usZVxnk
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP772943.RARMzQg1X1thD5KC3IoOLAo6F-HgH-F0vQ9NY7usZVxnk130_head
{
this:
np:hasAssertion
dgn-np:NP772943.RARMzQg1X1thD5KC3IoOLAo6F-HgH-F0vQ9NY7usZVxnk130_assertion
;
np:hasProvenance
dgn-np:NP772943.RARMzQg1X1thD5KC3IoOLAo6F-HgH-F0vQ9NY7usZVxnk130_provenance
;
np:hasPublicationInfo
dgn-np:NP772943.RARMzQg1X1thD5KC3IoOLAo6F-HgH-F0vQ9NY7usZVxnk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP772943.RARMzQg1X1thD5KC3IoOLAo6F-HgH-F0vQ9NY7usZVxnk130_assertion
a
np:Assertion
.
dgn-np:NP772943.RARMzQg1X1thD5KC3IoOLAo6F-HgH-F0vQ9NY7usZVxnk130_provenance
a
np:Provenance
.
dgn-np:NP772943.RARMzQg1X1thD5KC3IoOLAo6F-HgH-F0vQ9NY7usZVxnk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP772943.RARMzQg1X1thD5KC3IoOLAo6F-HgH-F0vQ9NY7usZVxnk130_assertion
{
miriam-gene:6262
a
ncit:C16612
.
lld:C0018801
a
ncit:C7057
.
dgn-gda:DGNb02a99fc4aecb44945569ffacad70710
sio:SIO_000628
miriam-gene:6262
,
lld:C0018801
;
a
sio:SIO_001121
.
}
dgn-np:NP772943.RARMzQg1X1thD5KC3IoOLAo6F-HgH-F0vQ9NY7usZVxnk130_provenance
{
dgn-np:NP772943.RARMzQg1X1thD5KC3IoOLAo6F-HgH-F0vQ9NY7usZVxnk130_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-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP772943.RARMzQg1X1thD5KC3IoOLAo6F-HgH-F0vQ9NY7usZVxnk130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:47:35+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}