@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP216070.RAvayK0q9jlx-AAvH3yZlH6qW5qlLv35bPxwtGUoBfB_Q
> .
@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:NP216070.RAvayK0q9jlx-AAvH3yZlH6qW5qlLv35bPxwtGUoBfB_Q130_head
{
this:
np:hasAssertion
dgn-np:NP216070.RAvayK0q9jlx-AAvH3yZlH6qW5qlLv35bPxwtGUoBfB_Q130_assertion
;
np:hasProvenance
dgn-np:NP216070.RAvayK0q9jlx-AAvH3yZlH6qW5qlLv35bPxwtGUoBfB_Q130_provenance
;
np:hasPublicationInfo
dgn-np:NP216070.RAvayK0q9jlx-AAvH3yZlH6qW5qlLv35bPxwtGUoBfB_Q130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP216070.RAvayK0q9jlx-AAvH3yZlH6qW5qlLv35bPxwtGUoBfB_Q130_assertion
a
np:Assertion
.
dgn-np:NP216070.RAvayK0q9jlx-AAvH3yZlH6qW5qlLv35bPxwtGUoBfB_Q130_provenance
a
np:Provenance
.
dgn-np:NP216070.RAvayK0q9jlx-AAvH3yZlH6qW5qlLv35bPxwtGUoBfB_Q130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP216070.RAvayK0q9jlx-AAvH3yZlH6qW5qlLv35bPxwtGUoBfB_Q130_assertion
{
miriam-gene:6331
a
ncit:C16612
.
lld:C0007193
a
ncit:C7057
.
dgn-gda:DGNbfc535787dd303b2572998a48a3cd0ec
sio:SIO_000628
miriam-gene:6331
,
lld:C0007193
;
a
sio:SIO_001121
.
}
dgn-np:NP216070.RAvayK0q9jlx-AAvH3yZlH6qW5qlLv35bPxwtGUoBfB_Q130_provenance
{
dgn-np:NP216070.RAvayK0q9jlx-AAvH3yZlH6qW5qlLv35bPxwtGUoBfB_Q130_assertion
dcterms:description
"[Since the identification of the first SCN5A mutation associated with long QT syndrome in 1995, several mutations in this gene for the alpha subunit of the cardiac sodium channel have been identified in a heterogeneous subset of cardiac rhythm syndromes, including Brugada syndrome, progressive cardiac conduction defect, sick sinus node syndrome, atrial fibrillation and dilated cardiomyopathy.]. 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:19377496
;
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:NP216070.RAvayK0q9jlx-AAvH3yZlH6qW5qlLv35bPxwtGUoBfB_Q130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:00+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" .
}