@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP648070.RAdE54owVePsINlj38KssniypcHr-4TFyb07V3dXaYLHY
> .
@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:NP648070.RAdE54owVePsINlj38KssniypcHr-4TFyb07V3dXaYLHY130_head
{
this:
np:hasAssertion
dgn-np:NP648070.RAdE54owVePsINlj38KssniypcHr-4TFyb07V3dXaYLHY130_assertion
;
np:hasProvenance
dgn-np:NP648070.RAdE54owVePsINlj38KssniypcHr-4TFyb07V3dXaYLHY130_provenance
;
np:hasPublicationInfo
dgn-np:NP648070.RAdE54owVePsINlj38KssniypcHr-4TFyb07V3dXaYLHY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP648070.RAdE54owVePsINlj38KssniypcHr-4TFyb07V3dXaYLHY130_assertion
a
np:Assertion
.
dgn-np:NP648070.RAdE54owVePsINlj38KssniypcHr-4TFyb07V3dXaYLHY130_provenance
a
np:Provenance
.
dgn-np:NP648070.RAdE54owVePsINlj38KssniypcHr-4TFyb07V3dXaYLHY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP648070.RAdE54owVePsINlj38KssniypcHr-4TFyb07V3dXaYLHY130_assertion
{
miriam-gene:3784
a
ncit:C16612
.
lld:C0040479
a
ncit:C7057
.
dgn-gda:DGNa2dd973ae8d3642230bbbd55fa46c66e
sio:SIO_000628
miriam-gene:3784
,
lld:C0040479
;
a
sio:SIO_001121
.
}
dgn-np:NP648070.RAdE54owVePsINlj38KssniypcHr-4TFyb07V3dXaYLHY130_provenance
{
dgn-np:NP648070.RAdE54owVePsINlj38KssniypcHr-4TFyb07V3dXaYLHY130_assertion
dcterms:description
"[KCNQ1 and KCNH2 are the two most common potassium channel genes causing long QT syndrome (LQTS), an inherited cardiac arrhythmia featured by QT prolongation and increased risks of developing torsade de pointes and sudden death.]. 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:18808722
;
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:NP648070.RAdE54owVePsINlj38KssniypcHr-4TFyb07V3dXaYLHY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:30+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" .
}