@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP593662.RANy0He2dI2BpGHyGe_6TstvWJj-uXpC_ojZBAYtkuZto> .
@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:NP593662.RANy0He2dI2BpGHyGe_6TstvWJj-uXpC_ojZBAYtkuZto130_head {
  this: np:hasAssertion dgn-np:NP593662.RANy0He2dI2BpGHyGe_6TstvWJj-uXpC_ojZBAYtkuZto130_assertion;
    np:hasProvenance dgn-np:NP593662.RANy0He2dI2BpGHyGe_6TstvWJj-uXpC_ojZBAYtkuZto130_provenance;
    np:hasPublicationInfo dgn-np:NP593662.RANy0He2dI2BpGHyGe_6TstvWJj-uXpC_ojZBAYtkuZto130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP593662.RANy0He2dI2BpGHyGe_6TstvWJj-uXpC_ojZBAYtkuZto130_assertion a np:Assertion .
  
  dgn-np:NP593662.RANy0He2dI2BpGHyGe_6TstvWJj-uXpC_ojZBAYtkuZto130_provenance a np:Provenance .
  
  dgn-np:NP593662.RANy0He2dI2BpGHyGe_6TstvWJj-uXpC_ojZBAYtkuZto130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP593662.RANy0He2dI2BpGHyGe_6TstvWJj-uXpC_ojZBAYtkuZto130_assertion {
  miriam-gene:920 a ncit:C16612 .
  
  lld:C0393819 a ncit:C7057 .
  
  dgn-gda:DGNb94a75600ec8ac28e6e46a8ad13906bc sio:SIO_000628 miriam-gene:920, lld:C0393819;
    a sio:SIO_001121 .
}

dgn-np:NP593662.RANy0He2dI2BpGHyGe_6TstvWJj-uXpC_ojZBAYtkuZto130_provenance {
  dgn-np:NP593662.RANy0He2dI2BpGHyGe_6TstvWJj-uXpC_ojZBAYtkuZto130_assertion dcterms:description
      "[Electrophysiological studies disclosed a reduction of nerve conduction velocity in both patients that was consistent with the diagnosis of chronic inflammatory demyelinating polyneuropathy (CIDP).This diagnosis was supported by histological demyelination in nerve biopsy specimens with patchy CD4, CD8 and CD68-positive cell infiltration in the first patient and increased protein content in the cerebrospinal fluid in the second patient.]. 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:18461357;
    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:NP593662.RANy0He2dI2BpGHyGe_6TstvWJj-uXpC_ojZBAYtkuZto130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:57+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" .
}