@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1398824.RAXKDUeY-EV-rPsi9kTIFow1HSkwtG_Q-0Uj-OM-7hK1w
> .
@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:NP1398824.RAXKDUeY-EV-rPsi9kTIFow1HSkwtG_Q-0Uj-OM-7hK1w130_head
{
this:
np:hasAssertion
dgn-np:NP1398824.RAXKDUeY-EV-rPsi9kTIFow1HSkwtG_Q-0Uj-OM-7hK1w130_assertion
;
np:hasProvenance
dgn-np:NP1398824.RAXKDUeY-EV-rPsi9kTIFow1HSkwtG_Q-0Uj-OM-7hK1w130_provenance
;
np:hasPublicationInfo
dgn-np:NP1398824.RAXKDUeY-EV-rPsi9kTIFow1HSkwtG_Q-0Uj-OM-7hK1w130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1398824.RAXKDUeY-EV-rPsi9kTIFow1HSkwtG_Q-0Uj-OM-7hK1w130_assertion
a
np:Assertion
.
dgn-np:NP1398824.RAXKDUeY-EV-rPsi9kTIFow1HSkwtG_Q-0Uj-OM-7hK1w130_provenance
a
np:Provenance
.
dgn-np:NP1398824.RAXKDUeY-EV-rPsi9kTIFow1HSkwtG_Q-0Uj-OM-7hK1w130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1398824.RAXKDUeY-EV-rPsi9kTIFow1HSkwtG_Q-0Uj-OM-7hK1w130_assertion
{
miriam-gene:6331
a
ncit:C16612
.
lld:C1141890
a
ncit:C7057
.
dgn-gda:DGN8052302bc4c7006daac13c725b0b9dae
sio:SIO_000628
miriam-gene:6331
,
lld:C1141890
;
a
sio:SIO_001121
.
}
dgn-np:NP1398824.RAXKDUeY-EV-rPsi9kTIFow1HSkwtG_Q-0Uj-OM-7hK1w130_provenance
{
dgn-np:NP1398824.RAXKDUeY-EV-rPsi9kTIFow1HSkwtG_Q-0Uj-OM-7hK1w130_assertion
dcterms:description
"[Inherited long QT syndrome (LQTS) recently has been associated with mutations in genes coding for potassium (KVLQT1, KCNE1, and HERG) or sodium (SCN5A) ion channels involved in regulating either sodium inward or potassium outward currents of heart cells, resulting in prolongation of the repolarization period.]. 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:9654228
;
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:NP1398824.RAXKDUeY-EV-rPsi9kTIFow1HSkwtG_Q-0Uj-OM-7hK1w130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:52:20+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: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" .
}