@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP541003.RAXJ5ZhyQpdQUixTf13wKir7djOtfLhH51f1qKUaISisc
> .
@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:NP541003.RAXJ5ZhyQpdQUixTf13wKir7djOtfLhH51f1qKUaISisc130_head
{
this:
np:hasAssertion
dgn-np:NP541003.RAXJ5ZhyQpdQUixTf13wKir7djOtfLhH51f1qKUaISisc130_assertion
;
np:hasProvenance
dgn-np:NP541003.RAXJ5ZhyQpdQUixTf13wKir7djOtfLhH51f1qKUaISisc130_provenance
;
np:hasPublicationInfo
dgn-np:NP541003.RAXJ5ZhyQpdQUixTf13wKir7djOtfLhH51f1qKUaISisc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP541003.RAXJ5ZhyQpdQUixTf13wKir7djOtfLhH51f1qKUaISisc130_assertion
a
np:Assertion
.
dgn-np:NP541003.RAXJ5ZhyQpdQUixTf13wKir7djOtfLhH51f1qKUaISisc130_provenance
a
np:Provenance
.
dgn-np:NP541003.RAXJ5ZhyQpdQUixTf13wKir7djOtfLhH51f1qKUaISisc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP541003.RAXJ5ZhyQpdQUixTf13wKir7djOtfLhH51f1qKUaISisc130_assertion
{
miriam-gene:6584
a
ncit:C16612
.
lld:C0002895
a
ncit:C7057
.
dgn-gda:DGNfd6db9ab6fa454467262e44b90a504ad
sio:SIO_000628
miriam-gene:6584
,
lld:C0002895
;
a
sio:SIO_001121
.
}
dgn-np:NP541003.RAXJ5ZhyQpdQUixTf13wKir7djOtfLhH51f1qKUaISisc130_provenance
{
dgn-np:NP541003.RAXJ5ZhyQpdQUixTf13wKir7djOtfLhH51f1qKUaISisc130_assertion
dcterms:description
"[Since genetic alterations in these genes underlie congenital long QT syndrome (LQTS), which is associated with an increased occurrence of arrhythmic complications and SCD, we decided to verify how alterations in these genes contribute to QT interval abnormalities and consequently to VA, SCA and SCD in post-MI patients.]. 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:18803136
;
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:NP541003.RAXJ5ZhyQpdQUixTf13wKir7djOtfLhH51f1qKUaISisc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:26+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" .
}