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

vh8:-JFDJHJTQ-4
  skos:prefLabel "maladie congénitale"@fr, "congenital disease"@en ;
  a skos:Concept ;
  skos:narrower vh8:-QBDZS657-P .

vh8:-QBDZS657-P
  skos:broader vh8:-N32K7HZ8-D, vh8:-LFCRK960-N, vh8:-JFDJHJTQ-4 ;
  a skos:Concept ;
  skos:prefLabel "Leber amaurosis"@en, "amaurose congénitale de Leber"@fr ;
  skos:exactMatch <https://en.wikipedia.org/wiki/Leber%27s_congenital_amaurosis>, <https://fr.wikipedia.org/wiki/Amaurose_cong%C3%A9nitale_de_Leber> ;
  skos:definition "Leber congenital amaurosis (LCA) is a rare inherited eye disease that appears at birth or in the first few months of life.One form of LCA was successfully treated with gene therapy in 2008.It affects about 1 in 40,000 newborns. (Wikipedia)"@en, "L'amaurose congénitale de Leber est une maladie génétique grave de la rétine décrit pour la première fois en 1869 par Théodor Leber qu'il appelle rétinite pigmentaire in utero. (Wikipédia)"@fr ;
  skos:narrower vh8:-FTMPWTHL-L ;
  skos:inScheme vh8: .

vh8: a skos:ConceptScheme .
vh8:-N32K7HZ8-D
  skos:prefLabel "hereditary disease"@en, "maladie héréditaire"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-QBDZS657-P .

vh8:-FTMPWTHL-L
  skos:prefLabel "syndrome de Senior-Loken"@fr, "Senior-Loken syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-QBDZS657-P .

vh8:-LFCRK960-N
  skos:prefLabel "retinopathy"@en, "rétinopathie"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-QBDZS657-P .