@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP362009.RAEgdgd4fHZ-Zj2EA3JMRmakr0yMCsxbmSzHOg4EslhGg
> .
@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:NP362009.RAEgdgd4fHZ-Zj2EA3JMRmakr0yMCsxbmSzHOg4EslhGg130_head
{
this:
np:hasAssertion
dgn-np:NP362009.RAEgdgd4fHZ-Zj2EA3JMRmakr0yMCsxbmSzHOg4EslhGg130_assertion
;
np:hasProvenance
dgn-np:NP362009.RAEgdgd4fHZ-Zj2EA3JMRmakr0yMCsxbmSzHOg4EslhGg130_provenance
;
np:hasPublicationInfo
dgn-np:NP362009.RAEgdgd4fHZ-Zj2EA3JMRmakr0yMCsxbmSzHOg4EslhGg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP362009.RAEgdgd4fHZ-Zj2EA3JMRmakr0yMCsxbmSzHOg4EslhGg130_assertion
a
np:Assertion
.
dgn-np:NP362009.RAEgdgd4fHZ-Zj2EA3JMRmakr0yMCsxbmSzHOg4EslhGg130_provenance
a
np:Provenance
.
dgn-np:NP362009.RAEgdgd4fHZ-Zj2EA3JMRmakr0yMCsxbmSzHOg4EslhGg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP362009.RAEgdgd4fHZ-Zj2EA3JMRmakr0yMCsxbmSzHOg4EslhGg130_assertion
{
miriam-gene:4397
a
ncit:C16612
.
lld:C0011303
a
ncit:C7057
.
dgn-gda:DGNdf4a949fc037c17fc1de00d8e70cc491
sio:SIO_000628
miriam-gene:4397
,
lld:C0011303
;
a
sio:SIO_001121
.
}
dgn-np:NP362009.RAEgdgd4fHZ-Zj2EA3JMRmakr0yMCsxbmSzHOg4EslhGg130_provenance
{
dgn-np:NP362009.RAEgdgd4fHZ-Zj2EA3JMRmakr0yMCsxbmSzHOg4EslhGg130_assertion
dcterms:description
"[There is also evidence, in experimental models of demyelination and in post-mortem tissue from patients with multiple sclerosis, for dysregulation of sodium channel gene expression in the cell bodies of some neurons whose axons have been demyelinated, suggesting that an acquired channelopathy may contribute to the pathophysiology of demyelinating diseases such as multiple sclerosis.]. 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:11119683
;
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:NP362009.RAEgdgd4fHZ-Zj2EA3JMRmakr0yMCsxbmSzHOg4EslhGg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:32+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" .
}