@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP251326.RA8q5weCGzjiU2OHrdF7BS10IOTLlUm_D7IrpPuDxt6w8
> .
@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:NP251326.RA8q5weCGzjiU2OHrdF7BS10IOTLlUm_D7IrpPuDxt6w8130_head
{
this:
np:hasAssertion
dgn-np:NP251326.RA8q5weCGzjiU2OHrdF7BS10IOTLlUm_D7IrpPuDxt6w8130_assertion
;
np:hasProvenance
dgn-np:NP251326.RA8q5weCGzjiU2OHrdF7BS10IOTLlUm_D7IrpPuDxt6w8130_provenance
;
np:hasPublicationInfo
dgn-np:NP251326.RA8q5weCGzjiU2OHrdF7BS10IOTLlUm_D7IrpPuDxt6w8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP251326.RA8q5weCGzjiU2OHrdF7BS10IOTLlUm_D7IrpPuDxt6w8130_assertion
a
np:Assertion
.
dgn-np:NP251326.RA8q5weCGzjiU2OHrdF7BS10IOTLlUm_D7IrpPuDxt6w8130_provenance
a
np:Provenance
.
dgn-np:NP251326.RA8q5weCGzjiU2OHrdF7BS10IOTLlUm_D7IrpPuDxt6w8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP251326.RA8q5weCGzjiU2OHrdF7BS10IOTLlUm_D7IrpPuDxt6w8130_assertion
{
miriam-gene:3757
a
ncit:C16612
.
lld:C1141890
a
ncit:C7057
.
dgn-gda:DGN55c303d937df22367b8a4ab6412e1f74
sio:SIO_000628
miriam-gene:3757
,
lld:C1141890
;
a
sio:SIO_001121
.
}
dgn-np:NP251326.RA8q5weCGzjiU2OHrdF7BS10IOTLlUm_D7IrpPuDxt6w8130_provenance
{
dgn-np:NP251326.RA8q5weCGzjiU2OHrdF7BS10IOTLlUm_D7IrpPuDxt6w8130_assertion
dcterms:description
"[Congenital long-QT syndrome (LQTS) is caused by mutations of genes encoding the slow component of the delayed rectifier current (LQT1, LQT5), the rapid component of the delayed rectifier current (LQT2, LQT6), or the Na(+) current (LQT3), resulting in ST-T-wave abnormalities on the ECG.]. 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:11104743
;
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:NP251326.RA8q5weCGzjiU2OHrdF7BS10IOTLlUm_D7IrpPuDxt6w8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:20+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" .
}