@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP263427.RABDB7Re5AJ286goUALkTc-dM3D7F0YavpCwTJg1oQyt0
> .
@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:NP263427.RABDB7Re5AJ286goUALkTc-dM3D7F0YavpCwTJg1oQyt0130_head
{
this:
np:hasAssertion
dgn-np:NP263427.RABDB7Re5AJ286goUALkTc-dM3D7F0YavpCwTJg1oQyt0130_assertion
;
np:hasProvenance
dgn-np:NP263427.RABDB7Re5AJ286goUALkTc-dM3D7F0YavpCwTJg1oQyt0130_provenance
;
np:hasPublicationInfo
dgn-np:NP263427.RABDB7Re5AJ286goUALkTc-dM3D7F0YavpCwTJg1oQyt0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP263427.RABDB7Re5AJ286goUALkTc-dM3D7F0YavpCwTJg1oQyt0130_assertion
a
np:Assertion
.
dgn-np:NP263427.RABDB7Re5AJ286goUALkTc-dM3D7F0YavpCwTJg1oQyt0130_provenance
a
np:Provenance
.
dgn-np:NP263427.RABDB7Re5AJ286goUALkTc-dM3D7F0YavpCwTJg1oQyt0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP263427.RABDB7Re5AJ286goUALkTc-dM3D7F0YavpCwTJg1oQyt0130_assertion
{
miriam-gene:3757
a
ncit:C16612
.
lld:C0023976
a
ncit:C7057
.
dgn-gda:DGNf216f4f1aa2430e59aebf24370717c3a
sio:SIO_000628
miriam-gene:3757
,
lld:C0023976
;
a
sio:SIO_001121
.
}
dgn-np:NP263427.RABDB7Re5AJ286goUALkTc-dM3D7F0YavpCwTJg1oQyt0130_provenance
{
dgn-np:NP263427.RABDB7Re5AJ286goUALkTc-dM3D7F0YavpCwTJg1oQyt0130_assertion
dcterms:description
"[Background-In long-QT syndrome (LQTS), heterozygosity for a mutation in 1 of the K(+) channel genes leads to prolongation of the cardiac action potential, because the aberrant protein exhibits loss of function. HERG, which is involved in LQT2, is the gene encoding the rapid component of the delayed rectifier, I(Kr).]. 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:10491368
;
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:NP263427.RABDB7Re5AJ286goUALkTc-dM3D7F0YavpCwTJg1oQyt0130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:43:45+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" .
}