@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP521218.RA0u6JmHgfsWzwFerIMwyMshOSLZ6jz4pSAmWsD5XeGSQ
> .
@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:NP521218.RA0u6JmHgfsWzwFerIMwyMshOSLZ6jz4pSAmWsD5XeGSQ130_head
{
this:
np:hasAssertion
dgn-np:NP521218.RA0u6JmHgfsWzwFerIMwyMshOSLZ6jz4pSAmWsD5XeGSQ130_assertion
;
np:hasProvenance
dgn-np:NP521218.RA0u6JmHgfsWzwFerIMwyMshOSLZ6jz4pSAmWsD5XeGSQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP521218.RA0u6JmHgfsWzwFerIMwyMshOSLZ6jz4pSAmWsD5XeGSQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP521218.RA0u6JmHgfsWzwFerIMwyMshOSLZ6jz4pSAmWsD5XeGSQ130_assertion
a
np:Assertion
.
dgn-np:NP521218.RA0u6JmHgfsWzwFerIMwyMshOSLZ6jz4pSAmWsD5XeGSQ130_provenance
a
np:Provenance
.
dgn-np:NP521218.RA0u6JmHgfsWzwFerIMwyMshOSLZ6jz4pSAmWsD5XeGSQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP521218.RA0u6JmHgfsWzwFerIMwyMshOSLZ6jz4pSAmWsD5XeGSQ130_assertion
{
miriam-gene:6262
a
ncit:C16612
.
lld:C0018799
a
ncit:C7057
.
dgn-gda:DGN1597ae57ed83011a42c8d46112f0884a
sio:SIO_000628
miriam-gene:6262
,
lld:C0018799
;
a
sio:SIO_001121
.
}
dgn-np:NP521218.RA0u6JmHgfsWzwFerIMwyMshOSLZ6jz4pSAmWsD5XeGSQ130_provenance
{
dgn-np:NP521218.RA0u6JmHgfsWzwFerIMwyMshOSLZ6jz4pSAmWsD5XeGSQ130_assertion
dcterms:description
"[CPVT patients with RYR2 mutation have bradycardia regardless of the site of the mutation, which could direct molecular diagnosis in (young) patients without structural heart disease presenting with syncopal events and a slow heart rate but with normal QTc at resting ECG.]. 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:16272262
;
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:NP521218.RA0u6JmHgfsWzwFerIMwyMshOSLZ6jz4pSAmWsD5XeGSQ130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:41+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: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" .
}