@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP753920.RAXiQkKdHibBLPDY3CrX71xI33CMUchQNNvd8nu88HGHU
> .
@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:NP753920.RAXiQkKdHibBLPDY3CrX71xI33CMUchQNNvd8nu88HGHU130_head
{
this:
np:hasAssertion
dgn-np:NP753920.RAXiQkKdHibBLPDY3CrX71xI33CMUchQNNvd8nu88HGHU130_assertion
;
np:hasProvenance
dgn-np:NP753920.RAXiQkKdHibBLPDY3CrX71xI33CMUchQNNvd8nu88HGHU130_provenance
;
np:hasPublicationInfo
dgn-np:NP753920.RAXiQkKdHibBLPDY3CrX71xI33CMUchQNNvd8nu88HGHU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP753920.RAXiQkKdHibBLPDY3CrX71xI33CMUchQNNvd8nu88HGHU130_assertion
a
np:Assertion
.
dgn-np:NP753920.RAXiQkKdHibBLPDY3CrX71xI33CMUchQNNvd8nu88HGHU130_provenance
a
np:Provenance
.
dgn-np:NP753920.RAXiQkKdHibBLPDY3CrX71xI33CMUchQNNvd8nu88HGHU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP753920.RAXiQkKdHibBLPDY3CrX71xI33CMUchQNNvd8nu88HGHU130_assertion
{
miriam-gene:6319
a
ncit:C16612
.
lld:C0040479
a
ncit:C7057
.
dgn-gda:DGNcb40ac4d6a6548acee595c77e18c00ed
sio:SIO_000628
miriam-gene:6319
,
lld:C0040479
;
a
sio:SIO_001121
.
}
dgn-np:NP753920.RAXiQkKdHibBLPDY3CrX71xI33CMUchQNNvd8nu88HGHU130_provenance
{
dgn-np:NP753920.RAXiQkKdHibBLPDY3CrX71xI33CMUchQNNvd8nu88HGHU130_assertion
dcterms:description
"[One of the most important and challenging aspects of caring for patients with congenital long QT syndrome (LQTS) is assessing an individual's risk of sudden cardiac death (SCD) because of torsades de pointes.]. 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:21907997
;
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:NP753920.RAXiQkKdHibBLPDY3CrX71xI33CMUchQNNvd8nu88HGHU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:36+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" .
}