@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP920809.RA9A8NLjx2-s-j3OgsgU-8mZdhqAQOw0baHbqXuhUGlAI> .
@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:NP920809.RA9A8NLjx2-s-j3OgsgU-8mZdhqAQOw0baHbqXuhUGlAI130_head {
  this: np:hasAssertion dgn-np:NP920809.RA9A8NLjx2-s-j3OgsgU-8mZdhqAQOw0baHbqXuhUGlAI130_assertion ;
    np:hasProvenance dgn-np:NP920809.RA9A8NLjx2-s-j3OgsgU-8mZdhqAQOw0baHbqXuhUGlAI130_provenance ;
    np:hasPublicationInfo dgn-np:NP920809.RA9A8NLjx2-s-j3OgsgU-8mZdhqAQOw0baHbqXuhUGlAI130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP920809.RA9A8NLjx2-s-j3OgsgU-8mZdhqAQOw0baHbqXuhUGlAI130_assertion a np:Assertion .
  dgn-np:NP920809.RA9A8NLjx2-s-j3OgsgU-8mZdhqAQOw0baHbqXuhUGlAI130_provenance a np:Provenance .
  dgn-np:NP920809.RA9A8NLjx2-s-j3OgsgU-8mZdhqAQOw0baHbqXuhUGlAI130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP920809.RA9A8NLjx2-s-j3OgsgU-8mZdhqAQOw0baHbqXuhUGlAI130_assertion {
  miriam-gene:23101 a ncit:C16612 .
  lld:C0027819 a ncit:C7057 .
  dgn-gda:DGNfd027b8f691d163db9d211610c106332 sio:SIO_000628 miriam-gene:23101 , lld:C0027819 ;
    a sio:SIO_001121 .
}
dgn-np:NP920809.RA9A8NLjx2-s-j3OgsgU-8mZdhqAQOw0baHbqXuhUGlAI130_provenance {
  dgn-np:NP920809.RA9A8NLjx2-s-j3OgsgU-8mZdhqAQOw0baHbqXuhUGlAI130_assertion dcterms:description "[Viruses were propagated in the MeWo cell line from which cell-free virus was harvested and applied to the ND7/23-Nav1.8 rat DRG x mouse neuroblastoma hybrid cell line which showed constitutive expression of the exogenous Nav 1.8, and endogenous expression of Nav 1.6 and Nav 1.7 genes all encoding sodium ion channels the dysregulation of which is associated with a range of neuropathic pain syndromes.]. 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:23382806 ;
    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:NP920809.RA9A8NLjx2-s-j3OgsgU-8mZdhqAQOw0baHbqXuhUGlAI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:25+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> ;
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}