@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" .
}