@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1158407.RA3lw7ml8ysu-WiD9ZewS0BG8Z5J1yF7cJBZcsS20rQDY
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP1158407.RA3lw7ml8ysu-WiD9ZewS0BG8Z5J1yF7cJBZcsS20rQDY130_head
{
this:
np:hasAssertion
dgn-np:NP1158407.RA3lw7ml8ysu-WiD9ZewS0BG8Z5J1yF7cJBZcsS20rQDY130_assertion
;
np:hasProvenance
dgn-np:NP1158407.RA3lw7ml8ysu-WiD9ZewS0BG8Z5J1yF7cJBZcsS20rQDY130_provenance
;
np:hasPublicationInfo
dgn-np:NP1158407.RA3lw7ml8ysu-WiD9ZewS0BG8Z5J1yF7cJBZcsS20rQDY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1158407.RA3lw7ml8ysu-WiD9ZewS0BG8Z5J1yF7cJBZcsS20rQDY130_assertion
a
np:Assertion
.
dgn-np:NP1158407.RA3lw7ml8ysu-WiD9ZewS0BG8Z5J1yF7cJBZcsS20rQDY130_provenance
a
np:Provenance
.
dgn-np:NP1158407.RA3lw7ml8ysu-WiD9ZewS0BG8Z5J1yF7cJBZcsS20rQDY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1158407.RA3lw7ml8ysu-WiD9ZewS0BG8Z5J1yF7cJBZcsS20rQDY130_assertion
{
miriam-gene:6331
a
ncit:C16612
.
lld:C1142166
a
ncit:C7057
.
dgn-gda:DGN98b79c7d86ec12f553626b3c6b352571
sio:SIO_000628
miriam-gene:6331
,
lld:C1142166
;
a
sio:SIO_001121
.
}
dgn-np:NP1158407.RA3lw7ml8ysu-WiD9ZewS0BG8Z5J1yF7cJBZcsS20rQDY130_provenance
{
dgn-np:NP1158407.RA3lw7ml8ysu-WiD9ZewS0BG8Z5J1yF7cJBZcsS20rQDY130_assertion
dcterms:description
"[Taken together, we have shown how apparently benign SCN5A BrS mutations can lead to the ECG abnormalities seen in patients with BrS through an induced defect that is only present when the mutations are coexpressed with WT channels.]. 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:24573164
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1158407.RA3lw7ml8ysu-WiD9ZewS0BG8Z5J1yF7cJBZcsS20rQDY130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:50:31+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}