@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP585467.RAukcMC5058QeZo1YYe3tpJXnFH02EHg0DArXoLR9w8wM
> .
@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:NP585467.RAukcMC5058QeZo1YYe3tpJXnFH02EHg0DArXoLR9w8wM130_head
{
this:
np:hasAssertion
dgn-np:NP585467.RAukcMC5058QeZo1YYe3tpJXnFH02EHg0DArXoLR9w8wM130_assertion
;
np:hasProvenance
dgn-np:NP585467.RAukcMC5058QeZo1YYe3tpJXnFH02EHg0DArXoLR9w8wM130_provenance
;
np:hasPublicationInfo
dgn-np:NP585467.RAukcMC5058QeZo1YYe3tpJXnFH02EHg0DArXoLR9w8wM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP585467.RAukcMC5058QeZo1YYe3tpJXnFH02EHg0DArXoLR9w8wM130_assertion
a
np:Assertion
.
dgn-np:NP585467.RAukcMC5058QeZo1YYe3tpJXnFH02EHg0DArXoLR9w8wM130_provenance
a
np:Provenance
.
dgn-np:NP585467.RAukcMC5058QeZo1YYe3tpJXnFH02EHg0DArXoLR9w8wM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP585467.RAukcMC5058QeZo1YYe3tpJXnFH02EHg0DArXoLR9w8wM130_assertion
{
miriam-gene:3737
a
ncit:C16612
.
lld:C0004134
a
ncit:C7057
.
dgn-gda:DGNeeb96c40123e8275795e889ddd9de584
sio:SIO_000628
miriam-gene:3737
,
lld:C0004134
;
a
sio:SIO_001121
.
}
dgn-np:NP585467.RAukcMC5058QeZo1YYe3tpJXnFH02EHg0DArXoLR9w8wM130_provenance
{
dgn-np:NP585467.RAukcMC5058QeZo1YYe3tpJXnFH02EHg0DArXoLR9w8wM130_assertion
dcterms:description
"[Disruption of the expression, distribution, and density of these channels through deletion or mutation of the genes encoding these channels, Kcna1 and Kcna2, is associated with neurologic pathologies including epilepsy and ataxia in humans and in rodent models.]. 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:22612818
;
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:NP585467.RAukcMC5058QeZo1YYe3tpJXnFH02EHg0DArXoLR9w8wM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:52+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" .
}