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

vh8:-VSN2N43D-R
  skos:prefLabel "syndrome de Bloom"@fr, "Bloom syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-Z080LN2C-5 .

vh8:-NPMTDL9S-D
  skos:prefLabel "site fragile"@fr, "fragile site"@en ;
  a skos:Concept ;
  skos:broader vh8:-Z080LN2C-5 .

vh8: a skos:ConceptScheme .
vh8:-CR27D8H3-X
  skos:prefLabel "maladie génétique"@fr, "genetic disease"@en ;
  a skos:Concept ;
  skos:narrower vh8:-Z080LN2C-5 .

vh8:-RJPT8CP6-9
  skos:prefLabel "Nijmegen breakage syndrome"@en, "syndrome de Nimègue"@fr ;
  a skos:Concept ;
  skos:broader vh8:-Z080LN2C-5 .

vh8:-Z080LN2C-5
  skos:prefLabel "fragilité chromosomique"@fr, "chromosome fragility"@en ;
  skos:broader vh8:-CR27D8H3-X ;
  skos:narrower vh8:-VSN2N43D-R, vh8:-NPMTDL9S-D, vh8:-W8K8J6P8-3, vh8:-PJ9NN9VT-6, vh8:-RJPT8CP6-9 ;
  skos:inScheme vh8: ;
  a skos:Concept .

vh8:-W8K8J6P8-3
  skos:prefLabel "Fanconi anemia"@en, "anémie de Fanconi"@fr ;
  a skos:Concept ;
  skos:broader vh8:-Z080LN2C-5 .

vh8:-PJ9NN9VT-6
  skos:prefLabel "syndrome du chromosome X fragile"@fr, "fragile X syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-Z080LN2C-5 .