@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP674473.RAxpZ5xb6N0cgo7y21kgjDecKyxW50R6CmxZrQWbmFsPo
> .
@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:NP674473.RAxpZ5xb6N0cgo7y21kgjDecKyxW50R6CmxZrQWbmFsPo130_head
{
this:
np:hasAssertion
dgn-np:NP674473.RAxpZ5xb6N0cgo7y21kgjDecKyxW50R6CmxZrQWbmFsPo130_assertion
;
np:hasProvenance
dgn-np:NP674473.RAxpZ5xb6N0cgo7y21kgjDecKyxW50R6CmxZrQWbmFsPo130_provenance
;
np:hasPublicationInfo
dgn-np:NP674473.RAxpZ5xb6N0cgo7y21kgjDecKyxW50R6CmxZrQWbmFsPo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP674473.RAxpZ5xb6N0cgo7y21kgjDecKyxW50R6CmxZrQWbmFsPo130_assertion
a
np:Assertion
.
dgn-np:NP674473.RAxpZ5xb6N0cgo7y21kgjDecKyxW50R6CmxZrQWbmFsPo130_provenance
a
np:Provenance
.
dgn-np:NP674473.RAxpZ5xb6N0cgo7y21kgjDecKyxW50R6CmxZrQWbmFsPo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP674473.RAxpZ5xb6N0cgo7y21kgjDecKyxW50R6CmxZrQWbmFsPo130_assertion
{
miriam-gene:6331
a
ncit:C16612
.
lld:C0038644
a
ncit:C7057
.
dgn-gda:DGN0825d9419e1de604013bccf3344527f5
sio:SIO_000628
miriam-gene:6331
,
lld:C0038644
;
a
sio:SIO_001121
.
}
dgn-np:NP674473.RAxpZ5xb6N0cgo7y21kgjDecKyxW50R6CmxZrQWbmFsPo130_provenance
{
dgn-np:NP674473.RAxpZ5xb6N0cgo7y21kgjDecKyxW50R6CmxZrQWbmFsPo130_assertion
dcterms:description
"[Mutations in sodium channel alpha-subunit gene (SCN5A) result in multiple arrhythmic syndromes, including long QT3 (LQT3), Brugada syndrome (BS), an inherited cardiac conduction defect, sudden unexpected nocturnal death syndrome (SUNDS) and sudden infant death syndrome (SIDS), constituting a spectrum of disease entities termed Na+ channelopathies.]. 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:14753626
;
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:NP674473.RAxpZ5xb6N0cgo7y21kgjDecKyxW50R6CmxZrQWbmFsPo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:47+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
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"v2.1.0" .
}