@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP61113.RAT0CoeaxvOWkWAgVWyffv255Q-w0Jqn2V8BM5TqJlSoo
> .
@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:NP61113.RAT0CoeaxvOWkWAgVWyffv255Q-w0Jqn2V8BM5TqJlSoo130_head
{
this:
np:hasAssertion
dgn-np:NP61113.RAT0CoeaxvOWkWAgVWyffv255Q-w0Jqn2V8BM5TqJlSoo130_assertion
;
np:hasProvenance
dgn-np:NP61113.RAT0CoeaxvOWkWAgVWyffv255Q-w0Jqn2V8BM5TqJlSoo130_provenance
;
np:hasPublicationInfo
dgn-np:NP61113.RAT0CoeaxvOWkWAgVWyffv255Q-w0Jqn2V8BM5TqJlSoo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP61113.RAT0CoeaxvOWkWAgVWyffv255Q-w0Jqn2V8BM5TqJlSoo130_assertion
a
np:Assertion
.
dgn-np:NP61113.RAT0CoeaxvOWkWAgVWyffv255Q-w0Jqn2V8BM5TqJlSoo130_provenance
a
np:Provenance
.
dgn-np:NP61113.RAT0CoeaxvOWkWAgVWyffv255Q-w0Jqn2V8BM5TqJlSoo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP61113.RAT0CoeaxvOWkWAgVWyffv255Q-w0Jqn2V8BM5TqJlSoo130_assertion
{
miriam-gene:3784
a
ncit:C16612
.
lld:C0023976
a
ncit:C7057
.
dgn-gda:DGNf1b1bcf17719d22d258234f12cccc0f7
sio:SIO_000628
miriam-gene:3784
,
lld:C0023976
;
a
sio:SIO_001122
.
}
dgn-np:NP61113.RAT0CoeaxvOWkWAgVWyffv255Q-w0Jqn2V8BM5TqJlSoo130_provenance
{
dgn-np:NP61113.RAT0CoeaxvOWkWAgVWyffv255Q-w0Jqn2V8BM5TqJlSoo130_assertion
dcterms:description
"[The LQTS genotype, QTc duration, and follow-up were determined in 243 cases of LQTS caused by the KCNQ1 potassium channel gene mutations (LQT1), 209 cases of LQTS caused by the HERG potassium channel gene mutations (LQT2), and 81 cases of LQTS caused by the SCN5A sodium channel gene mutation (LQT3) gene carriers.]. 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:12849668
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP61113.RAT0CoeaxvOWkWAgVWyffv255Q-w0Jqn2V8BM5TqJlSoo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:29+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" .
}