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

vh8:-QF166PD6-3
  skos:prefLabel "syndactylie"@fr, "syndactyly"@en ;
  a skos:Concept ;
  skos:narrower vh8:-X8PGNTR2-N .

vh8: a skos:ConceptScheme .
vh8:-N32K7HZ8-D
  skos:prefLabel "hereditary disease"@en, "maladie héréditaire"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-X8PGNTR2-N .

vh8:-CZGBG75B-L
  skos:prefLabel "osteochondrodysplasia"@en, "ostéochondrodysplasie"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-X8PGNTR2-N .

vh8:-X8PGNTR2-N
  skos:definition "Sclerosteosis is an autosomal recessive disorder characterized by bone overgrowth. It was first described in 1958 but given the current name in 1967. Excessive bone formation is most prominent in the skull, mandible and tubular bones. (Wikipedia)"@en, "La sclérostéose est la forme la plus grave de la mutation du gène SOST situé sur le locus q12-q21 du chromosome 17 codant la sclérostine. (Wikipédia)"@fr ;
  a skos:Concept ;
  skos:prefLabel "sclérostéose"@fr, "sclerosteosis"@en ;
  skos:exactMatch <https://en.wikipedia.org/wiki/Sclerosteosis>, <https://fr.wikipedia.org/wiki/Scl%C3%A9rost%C3%A9ose>, <https://www.wikidata.org/wiki/Q3475955> ;
  skos:inScheme vh8: ;
  skos:broader vh8:-N32K7HZ8-D, vh8:-QF166PD6-3, vh8:-CZGBG75B-L .