@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP179787.RAgfPys7pPhHLeCVAw1iUjDwWb3YQ_6doSP9u0ELqatiU
> .
@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:NP179787.RAgfPys7pPhHLeCVAw1iUjDwWb3YQ_6doSP9u0ELqatiU130_head
{
this:
np:hasAssertion
dgn-np:NP179787.RAgfPys7pPhHLeCVAw1iUjDwWb3YQ_6doSP9u0ELqatiU130_assertion
;
np:hasProvenance
dgn-np:NP179787.RAgfPys7pPhHLeCVAw1iUjDwWb3YQ_6doSP9u0ELqatiU130_provenance
;
np:hasPublicationInfo
dgn-np:NP179787.RAgfPys7pPhHLeCVAw1iUjDwWb3YQ_6doSP9u0ELqatiU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP179787.RAgfPys7pPhHLeCVAw1iUjDwWb3YQ_6doSP9u0ELqatiU130_assertion
a
np:Assertion
.
dgn-np:NP179787.RAgfPys7pPhHLeCVAw1iUjDwWb3YQ_6doSP9u0ELqatiU130_provenance
a
np:Provenance
.
dgn-np:NP179787.RAgfPys7pPhHLeCVAw1iUjDwWb3YQ_6doSP9u0ELqatiU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP179787.RAgfPys7pPhHLeCVAw1iUjDwWb3YQ_6doSP9u0ELqatiU130_assertion
{
miriam-gene:3752
a
ncit:C16612
.
lld:C1142166
a
ncit:C7057
.
dgn-gda:DGN699c53caef89ff882d263f45db15527c
sio:SIO_000628
miriam-gene:3752
,
lld:C1142166
;
a
sio:SIO_001121
.
}
dgn-np:NP179787.RAgfPys7pPhHLeCVAw1iUjDwWb3YQ_6doSP9u0ELqatiU130_provenance
{
dgn-np:NP179787.RAgfPys7pPhHLeCVAw1iUjDwWb3YQ_6doSP9u0ELqatiU130_assertion
dcterms:description
"[To follow a candidate gene approach for the involvement of the KCND2 and KCND3 genes (Kv4.2 and Kv4.3) in the pathogenesis of the long QT syndrome (LQTS) and Brugada syndrome, it is necessary to determine the genomic organisation of KCND2 and KCND3.]. 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:10942109
;
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:NP179787.RAgfPys7pPhHLeCVAw1iUjDwWb3YQ_6doSP9u0ELqatiU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:37+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
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"v2.1.0" .
}