@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP983843.RAKnqsjwfVG9ejGNFfWG68J_UJAkGcxNKtoLdMRkk32HY
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP983843.RAKnqsjwfVG9ejGNFfWG68J_UJAkGcxNKtoLdMRkk32HY130_head
{
this:
np:hasAssertion
dgn-np:NP983843.RAKnqsjwfVG9ejGNFfWG68J_UJAkGcxNKtoLdMRkk32HY130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP983843.RAKnqsjwfVG9ejGNFfWG68J_UJAkGcxNKtoLdMRkk32HY130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP983843.RAKnqsjwfVG9ejGNFfWG68J_UJAkGcxNKtoLdMRkk32HY130_assertion
a
np:Assertion
.
dgn-np:NP983843.RAKnqsjwfVG9ejGNFfWG68J_UJAkGcxNKtoLdMRkk32HY130_provenance
a
np:Provenance
.
dgn-np:NP983843.RAKnqsjwfVG9ejGNFfWG68J_UJAkGcxNKtoLdMRkk32HY130_publicationInfo
a
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.
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dgn-np:NP983843.RAKnqsjwfVG9ejGNFfWG68J_UJAkGcxNKtoLdMRkk32HY130_assertion
{
miriam-gene:3736
a
ncit:C16612
.
lld:C0014544
a
ncit:C7057
.
dgn-gda:DGNb53395e13a03b338e996d365a2a11b7f
sio:SIO_000628
miriam-gene:3736
,
lld:C0014544
;
a
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.
}
dgn-np:NP983843.RAKnqsjwfVG9ejGNFfWG68J_UJAkGcxNKtoLdMRkk32HY130_provenance
{
dgn-np:NP983843.RAKnqsjwfVG9ejGNFfWG68J_UJAkGcxNKtoLdMRkk32HY130_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-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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 .
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dgn-np:NP983843.RAKnqsjwfVG9ejGNFfWG68J_UJAkGcxNKtoLdMRkk32HY130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:49:11+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
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pav:authoredBy
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> , <
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> , <
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> , <
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
"v4.0.0.0" .
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"v4.0.0" .
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