@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP574612.RAsewJ2wIUWf8LZoQ9puGWam67Vl4xv2Jut8udq4riJVs
> .
@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:NP574612.RAsewJ2wIUWf8LZoQ9puGWam67Vl4xv2Jut8udq4riJVs130_head
{
this:
np:hasAssertion
dgn-np:NP574612.RAsewJ2wIUWf8LZoQ9puGWam67Vl4xv2Jut8udq4riJVs130_assertion
;
np:hasProvenance
dgn-np:NP574612.RAsewJ2wIUWf8LZoQ9puGWam67Vl4xv2Jut8udq4riJVs130_provenance
;
np:hasPublicationInfo
dgn-np:NP574612.RAsewJ2wIUWf8LZoQ9puGWam67Vl4xv2Jut8udq4riJVs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP574612.RAsewJ2wIUWf8LZoQ9puGWam67Vl4xv2Jut8udq4riJVs130_assertion
a
np:Assertion
.
dgn-np:NP574612.RAsewJ2wIUWf8LZoQ9puGWam67Vl4xv2Jut8udq4riJVs130_provenance
a
np:Provenance
.
dgn-np:NP574612.RAsewJ2wIUWf8LZoQ9puGWam67Vl4xv2Jut8udq4riJVs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP574612.RAsewJ2wIUWf8LZoQ9puGWam67Vl4xv2Jut8udq4riJVs130_assertion
{
miriam-gene:761
a
ncit:C16612
.
lld:C0014544
a
ncit:C7057
.
dgn-gda:DGN4998738360cff2b8f0e828ca63883387
sio:SIO_000628
miriam-gene:761
,
lld:C0014544
;
a
sio:SIO_001121
.
}
dgn-np:NP574612.RAsewJ2wIUWf8LZoQ9puGWam67Vl4xv2Jut8udq4riJVs130_provenance
{
dgn-np:NP574612.RAsewJ2wIUWf8LZoQ9puGWam67Vl4xv2Jut8udq4riJVs130_assertion
dcterms:description
"[These data indicate that loss of K(V)1.1 from its normal localization in axons and terminals of the CA3 region results in increased excitability in the CA3 recurrent axon collateral system, perhaps contributing to the limbic and tonic-clonic components of the observed epileptic phenotype.]. 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:9581771
;
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:NP574612.RAsewJ2wIUWf8LZoQ9puGWam67Vl4xv2Jut8udq4riJVs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:46+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" .
}