@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP311291.RAX7fI6EXCwdrOLuMGnWa0qQ0Wcb1QLk78qRpvR8MBW4Y> .
@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:NP311291.RAX7fI6EXCwdrOLuMGnWa0qQ0Wcb1QLk78qRpvR8MBW4Y130_head {
  this: np:hasAssertion dgn-np:NP311291.RAX7fI6EXCwdrOLuMGnWa0qQ0Wcb1QLk78qRpvR8MBW4Y130_assertion;
    np:hasProvenance dgn-np:NP311291.RAX7fI6EXCwdrOLuMGnWa0qQ0Wcb1QLk78qRpvR8MBW4Y130_provenance;
    np:hasPublicationInfo dgn-np:NP311291.RAX7fI6EXCwdrOLuMGnWa0qQ0Wcb1QLk78qRpvR8MBW4Y130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP311291.RAX7fI6EXCwdrOLuMGnWa0qQ0Wcb1QLk78qRpvR8MBW4Y130_assertion a np:Assertion .
  
  dgn-np:NP311291.RAX7fI6EXCwdrOLuMGnWa0qQ0Wcb1QLk78qRpvR8MBW4Y130_provenance a np:Provenance .
  
  dgn-np:NP311291.RAX7fI6EXCwdrOLuMGnWa0qQ0Wcb1QLk78qRpvR8MBW4Y130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP311291.RAX7fI6EXCwdrOLuMGnWa0qQ0Wcb1QLk78qRpvR8MBW4Y130_assertion {
  miriam-gene:4397 a ncit:C16612 .
  
  lld:C0023520 a ncit:C7057 .
  
  dgn-gda:DGN66bb220c7165d788b7cdf37d80681efe sio:SIO_000628 miriam-gene:4397, lld:C0023520;
    a sio:SIO_001121 .
}

dgn-np:NP311291.RAX7fI6EXCwdrOLuMGnWa0qQ0Wcb1QLk78qRpvR8MBW4Y130_provenance {
  dgn-np:NP311291.RAX7fI6EXCwdrOLuMGnWa0qQ0Wcb1QLk78qRpvR8MBW4Y130_assertion dcterms:description
      "[Demyelination caused by injury or disease together with failure of myelin regeneration disrupts the rapid propagation of action potentials along nerve fibers, and is associated with acquired and inherited disorders, including devastating multiple sclerosis and leukodystrophies.]. 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:23494530;
    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:NP311291.RAX7fI6EXCwdrOLuMGnWa0qQ0Wcb1QLk78qRpvR8MBW4Y130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:58+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" .
}