@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP643803.RAOCRX-dAywKihu2AlX3VzLy9bu8CLi1V08zyTIPfZ5yM
> .
@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:NP643803.RAOCRX-dAywKihu2AlX3VzLy9bu8CLi1V08zyTIPfZ5yM130_head
{
this:
np:hasAssertion
dgn-np:NP643803.RAOCRX-dAywKihu2AlX3VzLy9bu8CLi1V08zyTIPfZ5yM130_assertion
;
np:hasProvenance
dgn-np:NP643803.RAOCRX-dAywKihu2AlX3VzLy9bu8CLi1V08zyTIPfZ5yM130_provenance
;
np:hasPublicationInfo
dgn-np:NP643803.RAOCRX-dAywKihu2AlX3VzLy9bu8CLi1V08zyTIPfZ5yM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP643803.RAOCRX-dAywKihu2AlX3VzLy9bu8CLi1V08zyTIPfZ5yM130_assertion
a
np:Assertion
.
dgn-np:NP643803.RAOCRX-dAywKihu2AlX3VzLy9bu8CLi1V08zyTIPfZ5yM130_provenance
a
np:Provenance
.
dgn-np:NP643803.RAOCRX-dAywKihu2AlX3VzLy9bu8CLi1V08zyTIPfZ5yM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP643803.RAOCRX-dAywKihu2AlX3VzLy9bu8CLi1V08zyTIPfZ5yM130_assertion
{
miriam-gene:6331
a
ncit:C16612
.
lld:C0038644
a
ncit:C7057
.
dgn-gda:DGNc86a21035120d7062fd78a03887f9268
sio:SIO_000628
miriam-gene:6331
,
lld:C0038644
;
a
sio:SIO_001121
.
}
dgn-np:NP643803.RAOCRX-dAywKihu2AlX3VzLy9bu8CLi1V08zyTIPfZ5yM130_provenance
{
dgn-np:NP643803.RAOCRX-dAywKihu2AlX3VzLy9bu8CLi1V08zyTIPfZ5yM130_assertion
dcterms:description
"[SCN5A mutations that cause similar channel dysfunction may also contribute to sudden infant death syndrome (SIDS) and other arrhythmias in newborns, but the prevalence, impact, and therapeutic management of SCN5A mutations may be distinct in infants compared with adults.]. 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:18060054
;
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:NP643803.RAOCRX-dAywKihu2AlX3VzLy9bu8CLi1V08zyTIPfZ5yM130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:46:37+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" .
}