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

vh8: a skos:ConceptScheme .
vh8:-N32K7HZ8-D
  skos:prefLabel "hereditary disease"@en, "maladie héréditaire"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-SV79FDHT-5 .

vh8:-CZGBG75B-L
  skos:prefLabel "osteochondrodysplasia"@en, "ostéochondrodysplasie"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-SV79FDHT-5 .

vh8:-SV79FDHT-5
  skos:inScheme vh8: ;
  skos:altLabel "ostéodysplastie"@fr ;
  skos:broader vh8:-CZGBG75B-L, vh8:-N32K7HZ8-D, vh8:-H62GCVJ7-L ;
  skos:exactMatch <https://en.wikipedia.org/wiki/Melnick%E2%80%93Needles_syndrome>, <https://fr.wikipedia.org/wiki/Syndrome_de_Melnick-Needles> ;
  skos:prefLabel "Melnick-Needles osteodysplasia"@en, "ostéodysplasie de Melnick-Needles"@fr ;
  a skos:Concept ;
  skos:definition "Melnick–Needles syndrome (MNS), also known as Melnick–Needles osteodysplasty, is an extremely rare congenital disorder that affects primarily bone development. (Wikipedia)"@en, "Le syndrome de Melnick-Needles fait partie du spectre phénotypique des ostéodysplasies fronto-oto-palato-digitales.  (Wikipédia)"@fr .

vh8:-H62GCVJ7-L
  skos:prefLabel "ostéodysplasie"@fr, "osteodysplasia"@en ;
  a skos:Concept ;
  skos:narrower vh8:-SV79FDHT-5 .