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

vh8:-QBHNZVRZ-P
  skos:prefLabel "xeroderma pigmentosum"@fr, "xeroderma pigmentosum"@en ;
  a skos:Concept ;
  skos:narrower vh8:-CP3JG72K-X .

vh8: a skos:ConceptScheme .
vh8:-CP3JG72K-X
  skos:definition "DeSanctis–Cacchione syndrome is an extremely rare disorder characterized by the skin and eye symptoms of xeroderma pigmentosum (XP) occurring in association with microcephaly, progressive mental retardation, retarded growth and sexual development, deafness, choreoathetosis, ataxia and quadriparesis. (Wikipedia)"@en ;
  a skos:Concept ;
  skos:inScheme vh8: ;
  skos:broader vh8:-QBHNZVRZ-P, vh8:-KPWN34BB-M, vh8:-NG5HSD17-L ;
  skos:prefLabel "syndrome de De Sanctis-Cacchione"@fr, "De Sanctis-Cacchione syndrome"@en ;
  skos:exactMatch <https://en.wikipedia.org/wiki/DeSanctis%E2%80%93Cacchione_syndrome> .

vh8:-NG5HSD17-L
  skos:prefLabel "trouble neurologique"@fr, "neurological disorder"@en ;
  a skos:Concept ;
  skos:narrower vh8:-CP3JG72K-X .

vh8:-KPWN34BB-M
  skos:prefLabel "maladie rare"@fr, "rare disease"@en ;
  a skos:Concept ;
  skos:narrower vh8:-CP3JG72K-X .