@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP295216.RAABf9vkRhqCQkqgqwzvwxsPEqqyDzu5ku2K9C-eBKebY> .
@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:NP295216.RAABf9vkRhqCQkqgqwzvwxsPEqqyDzu5ku2K9C-eBKebY130_head {
  this: np:hasAssertion dgn-np:NP295216.RAABf9vkRhqCQkqgqwzvwxsPEqqyDzu5ku2K9C-eBKebY130_assertion;
    np:hasProvenance dgn-np:NP295216.RAABf9vkRhqCQkqgqwzvwxsPEqqyDzu5ku2K9C-eBKebY130_provenance;
    np:hasPublicationInfo dgn-np:NP295216.RAABf9vkRhqCQkqgqwzvwxsPEqqyDzu5ku2K9C-eBKebY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP295216.RAABf9vkRhqCQkqgqwzvwxsPEqqyDzu5ku2K9C-eBKebY130_assertion a np:Assertion .
  
  dgn-np:NP295216.RAABf9vkRhqCQkqgqwzvwxsPEqqyDzu5ku2K9C-eBKebY130_provenance a np:Provenance .
  
  dgn-np:NP295216.RAABf9vkRhqCQkqgqwzvwxsPEqqyDzu5ku2K9C-eBKebY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP295216.RAABf9vkRhqCQkqgqwzvwxsPEqqyDzu5ku2K9C-eBKebY130_assertion {
  miriam-gene:4566 a ncit:C16612 .
  
  lld:C0014544 a ncit:C7057 .
  
  dgn-gda:DGN928bac56494500ee5b27ea3285f9fd52 sio:SIO_000628 miriam-gene:4566, lld:C0014544;
    a sio:SIO_001121 .
}

dgn-np:NP295216.RAABf9vkRhqCQkqgqwzvwxsPEqqyDzu5ku2K9C-eBKebY130_provenance {
  dgn-np:NP295216.RAABf9vkRhqCQkqgqwzvwxsPEqqyDzu5ku2K9C-eBKebY130_assertion dcterms:description
      "[Examination of DNA from the affected sibs showed no deletions in the mitochondrial DNA nor the mutations identified in the syndromes of mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes (MELAS) or myoclonus, and epilepsy associated with rugged-red fibers (MERRF).]. 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:7726239;
    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:NP295216.RAABf9vkRhqCQkqgqwzvwxsPEqqyDzu5ku2K9C-eBKebY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:48+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" .
}