@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP622352.RAF5XxD_OwMjR2UoOWnDM9tvh7WYHsHipCEIk6iz3aKSo
> .
@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:NP622352.RAF5XxD_OwMjR2UoOWnDM9tvh7WYHsHipCEIk6iz3aKSo130_head
{
this:
np:hasAssertion
dgn-np:NP622352.RAF5XxD_OwMjR2UoOWnDM9tvh7WYHsHipCEIk6iz3aKSo130_assertion
;
np:hasProvenance
dgn-np:NP622352.RAF5XxD_OwMjR2UoOWnDM9tvh7WYHsHipCEIk6iz3aKSo130_provenance
;
np:hasPublicationInfo
dgn-np:NP622352.RAF5XxD_OwMjR2UoOWnDM9tvh7WYHsHipCEIk6iz3aKSo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP622352.RAF5XxD_OwMjR2UoOWnDM9tvh7WYHsHipCEIk6iz3aKSo130_assertion
a
np:Assertion
.
dgn-np:NP622352.RAF5XxD_OwMjR2UoOWnDM9tvh7WYHsHipCEIk6iz3aKSo130_provenance
a
np:Provenance
.
dgn-np:NP622352.RAF5XxD_OwMjR2UoOWnDM9tvh7WYHsHipCEIk6iz3aKSo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP622352.RAF5XxD_OwMjR2UoOWnDM9tvh7WYHsHipCEIk6iz3aKSo130_assertion
{
miriam-gene:6331
a
ncit:C16612
.
lld:C0037052
a
ncit:C7057
.
dgn-gda:DGN0aee6f5d8df6e0ec5e094456e74f71ed
sio:SIO_000628
miriam-gene:6331
,
lld:C0037052
;
a
sio:SIO_001121
.
}
dgn-np:NP622352.RAF5XxD_OwMjR2UoOWnDM9tvh7WYHsHipCEIk6iz3aKSo130_provenance
{
dgn-np:NP622352.RAF5XxD_OwMjR2UoOWnDM9tvh7WYHsHipCEIk6iz3aKSo130_assertion
dcterms:description
"[Mutations in SCN5A, the gene encoding Na(v)1.5, have been linked to many cardiac phenotypes, including the congenital and acquired long QT syndrome, Brugada syndrome, conduction slowing, sick sinus 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:19744495
;
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:NP622352.RAF5XxD_OwMjR2UoOWnDM9tvh7WYHsHipCEIk6iz3aKSo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:16+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" .
}