@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP510712.RACSK052_-bQbpOmMiUZKGxAw-Hr4NQoRL55Li9ItdBYY
> .
@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:NP510712.RACSK052_-bQbpOmMiUZKGxAw-Hr4NQoRL55Li9ItdBYY130_head
{
this:
np:hasAssertion
dgn-np:NP510712.RACSK052_-bQbpOmMiUZKGxAw-Hr4NQoRL55Li9ItdBYY130_assertion
;
np:hasProvenance
dgn-np:NP510712.RACSK052_-bQbpOmMiUZKGxAw-Hr4NQoRL55Li9ItdBYY130_provenance
;
np:hasPublicationInfo
dgn-np:NP510712.RACSK052_-bQbpOmMiUZKGxAw-Hr4NQoRL55Li9ItdBYY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP510712.RACSK052_-bQbpOmMiUZKGxAw-Hr4NQoRL55Li9ItdBYY130_assertion
a
np:Assertion
.
dgn-np:NP510712.RACSK052_-bQbpOmMiUZKGxAw-Hr4NQoRL55Li9ItdBYY130_provenance
a
np:Provenance
.
dgn-np:NP510712.RACSK052_-bQbpOmMiUZKGxAw-Hr4NQoRL55Li9ItdBYY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP510712.RACSK052_-bQbpOmMiUZKGxAw-Hr4NQoRL55Li9ItdBYY130_assertion
{
miriam-gene:6331
a
ncit:C16612
.
lld:C1720983
a
ncit:C7057
.
dgn-gda:DGN299719cce4eb54167e8840c766bc435d
sio:SIO_000628
miriam-gene:6331
,
lld:C1720983
;
a
sio:SIO_001121
.
}
dgn-np:NP510712.RACSK052_-bQbpOmMiUZKGxAw-Hr4NQoRL55Li9ItdBYY130_provenance
{
dgn-np:NP510712.RACSK052_-bQbpOmMiUZKGxAw-Hr4NQoRL55Li9ItdBYY130_assertion
dcterms:description
"[The aim of the present study was to elucidate the molecular mechanism underlying the concomitant occurrence of cardiac conduction disease and long QT syndrome (LQT3), two SCN5A channelopathies that are explained by loss-of-function and gain-of-function, respectively, in the cardiac Na+ channel.]. 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:18065446
;
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:NP510712.RACSK052_-bQbpOmMiUZKGxAw-Hr4NQoRL55Li9ItdBYY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:04+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" .
}