@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP404302.RA5EcLICERPibMS_Umx9FCSpPi9bvoUWJVZjcIvAfG91c
> .
@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:NP404302.RA5EcLICERPibMS_Umx9FCSpPi9bvoUWJVZjcIvAfG91c130_head
{
this:
np:hasAssertion
dgn-np:NP404302.RA5EcLICERPibMS_Umx9FCSpPi9bvoUWJVZjcIvAfG91c130_assertion
;
np:hasProvenance
dgn-np:NP404302.RA5EcLICERPibMS_Umx9FCSpPi9bvoUWJVZjcIvAfG91c130_provenance
;
np:hasPublicationInfo
dgn-np:NP404302.RA5EcLICERPibMS_Umx9FCSpPi9bvoUWJVZjcIvAfG91c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP404302.RA5EcLICERPibMS_Umx9FCSpPi9bvoUWJVZjcIvAfG91c130_assertion
a
np:Assertion
.
dgn-np:NP404302.RA5EcLICERPibMS_Umx9FCSpPi9bvoUWJVZjcIvAfG91c130_provenance
a
np:Provenance
.
dgn-np:NP404302.RA5EcLICERPibMS_Umx9FCSpPi9bvoUWJVZjcIvAfG91c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP404302.RA5EcLICERPibMS_Umx9FCSpPi9bvoUWJVZjcIvAfG91c130_assertion
{
miriam-gene:3757
a
ncit:C16612
.
lld:C1859062
a
ncit:C7057
.
dgn-gda:DGNa1a283437da918e6db9e013345378455
sio:SIO_000628
miriam-gene:3757
,
lld:C1859062
;
a
sio:SIO_001121
.
}
dgn-np:NP404302.RA5EcLICERPibMS_Umx9FCSpPi9bvoUWJVZjcIvAfG91c130_provenance
{
dgn-np:NP404302.RA5EcLICERPibMS_Umx9FCSpPi9bvoUWJVZjcIvAfG91c130_assertion
dcterms:description
"[Our data suggest that the dynamic response of ventricular repolarization to sympathetic stimulation differs between LQT1, LQT2 and LQT3 syndromes, and may explain why the trigger of cardiac events differs between the genotypes.]. 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:12069453
;
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:NP404302.RA5EcLICERPibMS_Umx9FCSpPi9bvoUWJVZjcIvAfG91c130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:00+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" .
}