@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP528278.RAed24aLtaDtOLzfSHsWE6uQbCmsYMF5z6FuPBDt16MEM> .
@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:NP528278.RAed24aLtaDtOLzfSHsWE6uQbCmsYMF5z6FuPBDt16MEM130_head {
  this: np:hasAssertion dgn-np:NP528278.RAed24aLtaDtOLzfSHsWE6uQbCmsYMF5z6FuPBDt16MEM130_assertion;
    np:hasProvenance dgn-np:NP528278.RAed24aLtaDtOLzfSHsWE6uQbCmsYMF5z6FuPBDt16MEM130_provenance;
    np:hasPublicationInfo dgn-np:NP528278.RAed24aLtaDtOLzfSHsWE6uQbCmsYMF5z6FuPBDt16MEM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP528278.RAed24aLtaDtOLzfSHsWE6uQbCmsYMF5z6FuPBDt16MEM130_assertion a np:Assertion .
  
  dgn-np:NP528278.RAed24aLtaDtOLzfSHsWE6uQbCmsYMF5z6FuPBDt16MEM130_provenance a np:Provenance .
  
  dgn-np:NP528278.RAed24aLtaDtOLzfSHsWE6uQbCmsYMF5z6FuPBDt16MEM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP528278.RAed24aLtaDtOLzfSHsWE6uQbCmsYMF5z6FuPBDt16MEM130_assertion {
  miriam-gene:23101 a ncit:C16612 .
  
  lld:C0027796 a ncit:C7057 .
  
  dgn-gda:DGNcc07aff0e5736e93303fd5da2b366e8f sio:SIO_000628 miriam-gene:23101, lld:C0027796;
    a sio:SIO_001121 .
}

dgn-np:NP528278.RAed24aLtaDtOLzfSHsWE6uQbCmsYMF5z6FuPBDt16MEM130_provenance {
  dgn-np:NP528278.RAed24aLtaDtOLzfSHsWE6uQbCmsYMF5z6FuPBDt16MEM130_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:NP528278.RAed24aLtaDtOLzfSHsWE6uQbCmsYMF5z6FuPBDt16MEM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:19+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" .
}