@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP683228.RA-asfBBJSCv89pX_3A3vFMv0E0YPTUETvjz6H3HAbrNc
> .
@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/v3.0.0/void/
> .
dgn-np:NP683228.RA-asfBBJSCv89pX_3A3vFMv0E0YPTUETvjz6H3HAbrNc130_head
{
this:
np:hasAssertion
dgn-np:NP683228.RA-asfBBJSCv89pX_3A3vFMv0E0YPTUETvjz6H3HAbrNc130_assertion
;
np:hasProvenance
dgn-np:NP683228.RA-asfBBJSCv89pX_3A3vFMv0E0YPTUETvjz6H3HAbrNc130_provenance
;
np:hasPublicationInfo
dgn-np:NP683228.RA-asfBBJSCv89pX_3A3vFMv0E0YPTUETvjz6H3HAbrNc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP683228.RA-asfBBJSCv89pX_3A3vFMv0E0YPTUETvjz6H3HAbrNc130_assertion
a
np:Assertion
.
dgn-np:NP683228.RA-asfBBJSCv89pX_3A3vFMv0E0YPTUETvjz6H3HAbrNc130_provenance
a
np:Provenance
.
dgn-np:NP683228.RA-asfBBJSCv89pX_3A3vFMv0E0YPTUETvjz6H3HAbrNc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP683228.RA-asfBBJSCv89pX_3A3vFMv0E0YPTUETvjz6H3HAbrNc130_assertion
{
miriam-gene:6331
a
ncit:C16612
.
lld:C2930805
a
ncit:C7057
.
dgn-gda:DGN11b5a95c73e5089333567aa5caa33cd2
sio:SIO_000628
miriam-gene:6331
,
lld:C2930805
;
a
sio:SIO_001121
.
}
dgn-np:NP683228.RA-asfBBJSCv89pX_3A3vFMv0E0YPTUETvjz6H3HAbrNc130_provenance
{
dgn-np:NP683228.RA-asfBBJSCv89pX_3A3vFMv0E0YPTUETvjz6H3HAbrNc130_assertion
dcterms:description
"[Mutations in sodium channel alpha-subunit gene (SCN5A) result in multiple arrhythmic syndromes, including long QT3 (LQT3), Brugada syndrome (BS), an inherited cardiac conduction defect, sudden unexpected nocturnal death syndrome (SUNDS) and sudden infant death syndrome (SIDS), constituting a spectrum of disease entities termed Na+ channelopathies.]. 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:14753626
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP683228.RA-asfBBJSCv89pX_3A3vFMv0E0YPTUETvjz6H3HAbrNc130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:44:32+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}