@prefix vh8: <http://data.loterre.fr/ark:/67375/VH8> .
@prefix skos: <http://www.w3.org/2004/02/skos/core#> .

vh8:-ZV61M3J7-S
  skos:prefLabel "atrophie du nerf optique"@fr, "optic nerve atrophy"@en ;
  a skos:Concept ;
  skos:narrower vh8:-ZWPG9CNS-H .

vh8:-ZWPG9CNS-H
  skos:definition "Behr syndrome is characterized by the association of early-onset optic atrophy with spinocerebellar degeneration resulting in ataxia, pyramidal signs, peripheral neuropathy and developmental delay.Although it is an autosomal recessive disorder, heterozygotes may still manifest much attenuated symptoms. (Wikipedia)"@en ;
  a skos:Concept ;
  skos:inScheme vh8: ;
  skos:broader vh8:-ZV61M3J7-S, vh8:-HFVJ6MCG-6, vh8:-N32K7HZ8-D ;
  skos:prefLabel "syndrome de Behr"@fr, "Behr syndrome"@en ;
  skos:exactMatch <https://en.wikipedia.org/wiki/Behr_syndrome> .

vh8: a skos:ConceptScheme .
vh8:-N32K7HZ8-D
  skos:prefLabel "hereditary disease"@en, "maladie héréditaire"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-ZWPG9CNS-H .

vh8:-HFVJ6MCG-6
  skos:prefLabel "nervous system diseases"@en, "pathologie du système nerveux"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-ZWPG9CNS-H .