@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP209307.RAxyDrcuQLPIxASCqB1AcarRdTOaa0nNyDh_P1adQ8wqg
> .
@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:NP209307.RAxyDrcuQLPIxASCqB1AcarRdTOaa0nNyDh_P1adQ8wqg130_head
{
this:
np:hasAssertion
dgn-np:NP209307.RAxyDrcuQLPIxASCqB1AcarRdTOaa0nNyDh_P1adQ8wqg130_assertion
;
np:hasProvenance
dgn-np:NP209307.RAxyDrcuQLPIxASCqB1AcarRdTOaa0nNyDh_P1adQ8wqg130_provenance
;
np:hasPublicationInfo
dgn-np:NP209307.RAxyDrcuQLPIxASCqB1AcarRdTOaa0nNyDh_P1adQ8wqg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP209307.RAxyDrcuQLPIxASCqB1AcarRdTOaa0nNyDh_P1adQ8wqg130_assertion
a
np:Assertion
.
dgn-np:NP209307.RAxyDrcuQLPIxASCqB1AcarRdTOaa0nNyDh_P1adQ8wqg130_provenance
a
np:Provenance
.
dgn-np:NP209307.RAxyDrcuQLPIxASCqB1AcarRdTOaa0nNyDh_P1adQ8wqg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP209307.RAxyDrcuQLPIxASCqB1AcarRdTOaa0nNyDh_P1adQ8wqg130_assertion
{
miriam-gene:6331
a
ncit:C16612
.
lld:C0023976
a
ncit:C7057
.
dgn-gda:DGN6eb6aa843cc06e3950c87b26e67437ea
sio:SIO_000628
miriam-gene:6331
,
lld:C0023976
;
a
sio:SIO_001121
.
}
dgn-np:NP209307.RAxyDrcuQLPIxASCqB1AcarRdTOaa0nNyDh_P1adQ8wqg130_provenance
{
dgn-np:NP209307.RAxyDrcuQLPIxASCqB1AcarRdTOaa0nNyDh_P1adQ8wqg130_assertion
dcterms:description
"[On the other hand, mutations in another cardiac ion channel gene, SCN5A, also cause sinus node dysfunction as well as other cardiac arrhythmias, including long QT syndrome, Brugada syndrome, idiopathic ventricular fibrillation, and progressive cardiac conduction disturbance.]. 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:15123648
;
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:NP209307.RAxyDrcuQLPIxASCqB1AcarRdTOaa0nNyDh_P1adQ8wqg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:55+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" .
}