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

vh8:-PLFNN4S2-4
  skos:prefLabel "metabolic diseases"@en, "maladie métabolique"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-NNL526RR-H .

vh8: a skos:ConceptScheme .
vh8:-NNL526RR-H
  skos:exactMatch <https://fr.wikipedia.org/wiki/Amylose_de_la_transthyr%C3%A9tine>, <https://en.wikipedia.org/wiki/Familial_amyloid_polyneuropathy> ;
  skos:definition "Familial amyloid polyneuropathy, also called transthyretin-related hereditary amyloidosis, transthyretin amyloidosis abbreviated also as ATTR (hereditary form), or Corino de Andrade's disease, is an autosomal dominant neurodegenerative disease (Wikipedia)"@en, "L'amylose de la (ou à) transthyrétine ou amyloïdose de la transthyrétine, est une amyloïdose, maladie systémique caractérisée par une atteinte du système nerveux, des reins, des yeux et du cœur.  (Wikipédia)"@fr ;
  skos:altLabel "British type amyloidosis"@en, "Andrade's type of heritable polyneuropathy"@en, "Andrade's paramyeloidosis"@en, "neuropathic amyloid syndrome"@en, "Swedish type amyloidosis"@en, "hereditary neuropathic amyloidosis"@en, "Corino de Andrade syndrome"@en, "TTR abnormality"@en, "transhyretin abnormality"@en, "neuropathic hereditary amyloidosis"@en, "familial Portuguese polyneuritic amyloidosis"@en, "Portuguese type of hereditary neuropathic amyloidosis"@en, "Wohlwill-Corino Andrade syndrome"@en, "Japanese type amyloidosis"@en, "amyloid neuropathy type I"@en ;
  skos:prefLabel "polyneuropathie amyloïde familiale de type 1"@fr, "familial amyloidotic polyneuropathy type 1"@en ;
  a skos:Concept ;
  skos:inScheme vh8: ;
  skos:broader vh8:-PLFNN4S2-4, vh8:-HFVJ6MCG-6, vh8:-L115LG3M-0 .

vh8:-HFVJ6MCG-6
  skos:prefLabel "nervous system diseases"@en, "pathologie du système nerveux"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-NNL526RR-H .

vh8:-L115LG3M-0
  skos:prefLabel "polyneuropathie périphérique"@fr, "polyneuropathy"@en ;
  a skos:Concept ;
  skos:narrower vh8:-NNL526RR-H .