@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP476243.RARXrNPAyMF4nuhY4YIHfZIkbIsd0g8z1iujd_8AH--BM> .
@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:NP476243.RARXrNPAyMF4nuhY4YIHfZIkbIsd0g8z1iujd_8AH--BM130_head {
  this: np:hasAssertion dgn-np:NP476243.RARXrNPAyMF4nuhY4YIHfZIkbIsd0g8z1iujd_8AH--BM130_assertion ;
    np:hasProvenance dgn-np:NP476243.RARXrNPAyMF4nuhY4YIHfZIkbIsd0g8z1iujd_8AH--BM130_provenance ;
    np:hasPublicationInfo dgn-np:NP476243.RARXrNPAyMF4nuhY4YIHfZIkbIsd0g8z1iujd_8AH--BM130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP476243.RARXrNPAyMF4nuhY4YIHfZIkbIsd0g8z1iujd_8AH--BM130_assertion a np:Assertion .
  dgn-np:NP476243.RARXrNPAyMF4nuhY4YIHfZIkbIsd0g8z1iujd_8AH--BM130_provenance a np:Provenance .
  dgn-np:NP476243.RARXrNPAyMF4nuhY4YIHfZIkbIsd0g8z1iujd_8AH--BM130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP476243.RARXrNPAyMF4nuhY4YIHfZIkbIsd0g8z1iujd_8AH--BM130_assertion {
  miriam-gene:4566 a ncit:C16612 .
  lld:C0162671 a ncit:C7057 .
  dgn-gda:DGN685bb6c650ba4d9627eebbfc81c17a0e sio:SIO_000628 miriam-gene:4566 , lld:C0162671 ;
    a sio:SIO_001121 .
}
dgn-np:NP476243.RARXrNPAyMF4nuhY4YIHfZIkbIsd0g8z1iujd_8AH--BM130_provenance {
  dgn-np:NP476243.RARXrNPAyMF4nuhY4YIHfZIkbIsd0g8z1iujd_8AH--BM130_assertion dcterms:description "[Since modification of these taurine-containing uridines has been found to be lacking in mutant mitochondrial tRNAs for Leu(UUR) and Lys from pathogenic cells of the mitochondrial encephalomyopathies MELAS and MERRF, respectively, our findings will considerably deepen our understanding of the molecular pathogenesis of mitochondrial encephalomyopathic diseases.]. 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:12456664 ;
    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:NP476243.RARXrNPAyMF4nuhY4YIHfZIkbIsd0g8z1iujd_8AH--BM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:45+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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    pav:version "v2.1.0.0" .
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}