dgn-np:NP196429.RArD1JnFwkrG4noiAa446hT8GjqUgGnL44grdWIXw-jac130_provenance {
  dgn-np:NP196429.RArD1JnFwkrG4noiAa446hT8GjqUgGnL44grdWIXw-jac130_assertion dcterms:description "[A genetic linkage study was performed with markers spanning the Friedreich ataxia, Spastic ataxia of the Charlevoix-Saguenay, Autosomal recessive ataxia associated with isolated vitamin E deficiency, Ataxia with oculomotor apraxia, Infantile onset spinocerebellar ataxia, Ataxia with Hearing Loss and Optic Atrophy, AT, ATLD, Spinocerebellar ataxia with axonal neuropathy, Cayman ataxia, Cerebellar ataxia with mental retardation optic atrophy and skin abnormalities, Salla syndrome, Marinesco-Sjögren and the Childhood Spinocerebellar Ataxia loci.]. 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:16550933 ;
    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 .
}