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

vh8:-R99WQ5B2-D
  skos:prefLabel "chromosome anormal"@fr, "abnormal chromosome"@en ;
  a skos:Concept ;
  skos:narrower vh8:-S9HDWXHT-R .

vh8:-ZLR2Q92T-B
  skos:prefLabel "syndrome du gène contigu"@fr, "contiguous gene syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-S9HDWXHT-R .

vh8: a skos:ConceptScheme .
vh8:-S9HDWXHT-R
  a skos:Concept ;
  skos:prefLabel "deletion"@en, "délétion"@fr ;
  skos:exactMatch <https://fr.wikipedia.org/wiki/D%C3%A9l%C3%A9tion_(g%C3%A9n%C3%A9tique)>, <https://en.wikipedia.org/wiki/Deletion_(genetics)> ;
  skos:definition "In genetics, a deletion (also called gene deletion, deficiency, or deletion mutation) (sign: Δ) is a mutation (a genetic aberration) in which a part of a chromosome or a sequence of DNA is left out during DNA replication. Any number of nucleotides can be deleted, from a single base to an entire piece of chromosome. (Wikipedia)"@en, "La délétion (symbole: Δ) est une mutation génétique caractérisée par la perte de matériel génétique sur un chromosome. (Wikipédia)"@fr ;
  skos:narrower vh8:-ZLR2Q92T-B ;
  skos:inScheme vh8: ;
  skos:broader vh8:-R99WQ5B2-D .