@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP619198.RA70xToPh-qdqJYszh_8dJJftpCHRkbt4LBYtLEbKKnPo
> .
@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:NP619198.RA70xToPh-qdqJYszh_8dJJftpCHRkbt4LBYtLEbKKnPo130_head
{
this:
np:hasAssertion
dgn-np:NP619198.RA70xToPh-qdqJYszh_8dJJftpCHRkbt4LBYtLEbKKnPo130_assertion
;
np:hasProvenance
dgn-np:NP619198.RA70xToPh-qdqJYszh_8dJJftpCHRkbt4LBYtLEbKKnPo130_provenance
;
np:hasPublicationInfo
dgn-np:NP619198.RA70xToPh-qdqJYszh_8dJJftpCHRkbt4LBYtLEbKKnPo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP619198.RA70xToPh-qdqJYszh_8dJJftpCHRkbt4LBYtLEbKKnPo130_assertion
a
np:Assertion
.
dgn-np:NP619198.RA70xToPh-qdqJYszh_8dJJftpCHRkbt4LBYtLEbKKnPo130_provenance
a
np:Provenance
.
dgn-np:NP619198.RA70xToPh-qdqJYszh_8dJJftpCHRkbt4LBYtLEbKKnPo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP619198.RA70xToPh-qdqJYszh_8dJJftpCHRkbt4LBYtLEbKKnPo130_assertion
{
miriam-gene:3784
a
ncit:C16612
.
lld:C1859062
a
ncit:C7057
.
dgn-gda:DGNaca955061b674f418a32b3a5abe441ba
sio:SIO_000628
miriam-gene:3784
,
lld:C1859062
;
a
sio:SIO_001121
.
}
dgn-np:NP619198.RA70xToPh-qdqJYszh_8dJJftpCHRkbt4LBYtLEbKKnPo130_provenance
{
dgn-np:NP619198.RA70xToPh-qdqJYszh_8dJJftpCHRkbt4LBYtLEbKKnPo130_assertion
dcterms:description
"[A differential response of dynamic QT interval to epinephrine infusion between LQT1, LQT2, and LQT3 syndromes has been reported, indicating the potential diagnostic value of the epinephrine test for genotyping the three forms.]. 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:15851169
;
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:NP619198.RA70xToPh-qdqJYszh_8dJJftpCHRkbt4LBYtLEbKKnPo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:14+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" .
}