@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP573148.RAX60oEg66QqMI5wtHFlhCPgDEvK_fvci9nBB3tIkdk9g
> .
@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:NP573148.RAX60oEg66QqMI5wtHFlhCPgDEvK_fvci9nBB3tIkdk9g130_head
{
this:
np:hasAssertion
dgn-np:NP573148.RAX60oEg66QqMI5wtHFlhCPgDEvK_fvci9nBB3tIkdk9g130_assertion
;
np:hasProvenance
dgn-np:NP573148.RAX60oEg66QqMI5wtHFlhCPgDEvK_fvci9nBB3tIkdk9g130_provenance
;
np:hasPublicationInfo
dgn-np:NP573148.RAX60oEg66QqMI5wtHFlhCPgDEvK_fvci9nBB3tIkdk9g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP573148.RAX60oEg66QqMI5wtHFlhCPgDEvK_fvci9nBB3tIkdk9g130_assertion
a
np:Assertion
.
dgn-np:NP573148.RAX60oEg66QqMI5wtHFlhCPgDEvK_fvci9nBB3tIkdk9g130_provenance
a
np:Provenance
.
dgn-np:NP573148.RAX60oEg66QqMI5wtHFlhCPgDEvK_fvci9nBB3tIkdk9g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP573148.RAX60oEg66QqMI5wtHFlhCPgDEvK_fvci9nBB3tIkdk9g130_assertion
{
miriam-gene:3784
a
ncit:C16612
.
lld:C1141890
a
ncit:C7057
.
dgn-gda:DGN0aa5a78c55ce51d8a00d7e295cca2e0d
sio:SIO_000628
miriam-gene:3784
,
lld:C1141890
;
a
sio:SIO_001121
.
}
dgn-np:NP573148.RAX60oEg66QqMI5wtHFlhCPgDEvK_fvci9nBB3tIkdk9g130_provenance
{
dgn-np:NP573148.RAX60oEg66QqMI5wtHFlhCPgDEvK_fvci9nBB3tIkdk9g130_assertion
dcterms:description
"[The most prevalent LQT1 form of inherited long QT syndrome is caused by mutations of the KCNQ1 gene resulting repolarizing I(Ks) potassium current to decrease and the QT interval to prolong.]. 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:17023080
;
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:NP573148.RAX60oEg66QqMI5wtHFlhCPgDEvK_fvci9nBB3tIkdk9g130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:46:05+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" .
}