@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP716799.RAoIE6xo0DWGMhfM_ZKqCGzR1-4eXLhTzq-Q72jGEdyV4
> .
@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:NP716799.RAoIE6xo0DWGMhfM_ZKqCGzR1-4eXLhTzq-Q72jGEdyV4130_head
{
this:
np:hasAssertion
dgn-np:NP716799.RAoIE6xo0DWGMhfM_ZKqCGzR1-4eXLhTzq-Q72jGEdyV4130_assertion
;
np:hasProvenance
dgn-np:NP716799.RAoIE6xo0DWGMhfM_ZKqCGzR1-4eXLhTzq-Q72jGEdyV4130_provenance
;
np:hasPublicationInfo
dgn-np:NP716799.RAoIE6xo0DWGMhfM_ZKqCGzR1-4eXLhTzq-Q72jGEdyV4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP716799.RAoIE6xo0DWGMhfM_ZKqCGzR1-4eXLhTzq-Q72jGEdyV4130_assertion
a
np:Assertion
.
dgn-np:NP716799.RAoIE6xo0DWGMhfM_ZKqCGzR1-4eXLhTzq-Q72jGEdyV4130_provenance
a
np:Provenance
.
dgn-np:NP716799.RAoIE6xo0DWGMhfM_ZKqCGzR1-4eXLhTzq-Q72jGEdyV4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP716799.RAoIE6xo0DWGMhfM_ZKqCGzR1-4eXLhTzq-Q72jGEdyV4130_assertion
{
miriam-gene:55800
a
ncit:C16612
.
lld:C0232197
a
ncit:C7057
.
dgn-gda:DGN63a192dc17fad44f5f288c6d0629fc90
sio:SIO_000628
miriam-gene:55800
,
lld:C0232197
;
a
sio:SIO_001121
.
}
dgn-np:NP716799.RAoIE6xo0DWGMhfM_ZKqCGzR1-4eXLhTzq-Q72jGEdyV4130_provenance
{
dgn-np:NP716799.RAoIE6xo0DWGMhfM_ZKqCGzR1-4eXLhTzq-Q72jGEdyV4130_assertion
dcterms:description
"[Mutations in the cardiac sodium channel α, β1, β2 and β3 subunit genes (SCN5A, SCN1B, SCN2B and SCN3B) have been associated with AF, which suggests that mutations in the sodium channel β4 subunit gene, SCN4B, are also involved in the pathogenesis of AF.]. 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:23604097
;
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:NP716799.RAoIE6xo0DWGMhfM_ZKqCGzR1-4eXLhTzq-Q72jGEdyV4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:15+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" .
}