@prefix jvr: <http://data.loterre.fr/ark:/67375/JVR> .
@prefix skos: <http://www.w3.org/2004/02/skos/core#> .
@prefix mesh: <http://id.nlm.nih.gov/mesh/vocab#> .
@prefix dc: <http://purl.org/dc/terms/> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix owl: <http://www.w3.org/2002/07/owl#> .

jvr:-Z9TSGBXH-4
  skos:prefLabel "génétique (Qualificatif)"@fr, "genetics (Qualifier)"@en ;
  a mesh:Qualifier, skos:Concept .

jvr:-H7K65Q8S-Z
  skos:prefLabel "radiation effects (Qualifier)"@en, "effets des radiations (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-G9396H6L-R
  skos:prefLabel "Dystrophie myotonique"@fr, "Myotonic Dystrophy"@en ;
  a mesh:Descriptor, skos:Concept ;
  skos:related jvr:-NT58TNXQ-G .

jvr:-NT58TNXQ-G
  dc:modified "2016-06-17"^^xsd:date ;
  skos:prefLabel "Trinucleotide Repeat Expansion"@en, "Expansion de trinucléotide répété"@fr ;
  a mesh:Descriptor, skos:Concept ;
  skos:altLabel "Expansion de répétition de trinucléotide"@fr, "Expanded Trinucleotide Repeat"@en, "Répétition de trinucléotide expansée"@fr, "Expansion de triplet répété"@fr, "Expansion de répétition de triplet"@fr, "Répétition de triplet expansée"@fr ;
  skos:broader jvr:-MLD02K7C-B, jvr:-W6ZT3KKJ-N ;
  dc:established "1998-01-01"^^xsd:date ;
  owl:sameAs <http://id.nlm.nih.gov/mesh/D019680> ;
  skos:definition "An increased number of contiguous trinucleotide repeats in the DNA sequence from one generation to the next. The presence of these regions is associated with diseases such as FRAGILE X SYNDROME and MYOTONIC DYSTROPHY. Some CHROMOSOME FRAGILE SITES are composed of sequences where trinucleotide repeat expansion occurs."@en ;
  mesh:allowableQualifier jvr:-S0CS1X5R-5, jvr:-WZF2ZR3L-B, jvr:-PPKJKFKK-V, jvr:-N2WP45CN-V, jvr:-H7K65Q8S-Z, jvr:-Z9TSGBXH-4 ;
  skos:related jvr:-KZK3R3W2-V, jvr:-VWVSVF45-N, jvr:-G9396H6L-R, jvr:-QG1VF01W-T, jvr:-CGT2SN12-T ;
  dc:created "1997-06-20"^^xsd:date ;
  skos:inScheme jvr: .

jvr:-S0CS1X5R-5
  skos:prefLabel "immunology (Qualifier)"@en, "immunologie (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-N2WP45CN-V
  skos:prefLabel "drug effects (Qualifier)"@en, "effets des médicaments et des substances chimiques (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-KZK3R3W2-V
  skos:prefLabel "Fragile X Syndrome"@en, "Syndrome du chromosome X fragile"@fr ;
  a mesh:Descriptor, skos:Concept ;
  skos:related jvr:-NT58TNXQ-G .

jvr:-PPKJKFKK-V
  skos:prefLabel "ethics (Qualifier)"@en, "éthique (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-QG1VF01W-T
  skos:prefLabel "Anticipation génétique"@fr, "Anticipation, Genetic"@en ;
  a mesh:Descriptor, skos:Concept ;
  skos:related jvr:-NT58TNXQ-G .

jvr:-CGT2SN12-T
  skos:prefLabel "Chromosome Fragility"@en, "Fragilité des chromosomes"@fr ;
  a mesh:Descriptor, skos:Concept ;
  skos:related jvr:-NT58TNXQ-G .

jvr:-MLD02K7C-B
  skos:prefLabel "Expansion de séquence répétée de l'ADN"@fr, "DNA Repeat Expansion"@en ;
  a mesh:Descriptor, skos:Concept ;
  skos:narrower jvr:-NT58TNXQ-G .

jvr:-WZF2ZR3L-B
  skos:prefLabel "physiology (Qualifier)"@en, "physiologie (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr: a skos:ConceptScheme .
jvr:-VWVSVF45-N
  skos:prefLabel "Sites fragiles de chromosome"@fr, "Chromosome Fragile Sites"@en ;
  a mesh:Descriptor, skos:Concept ;
  skos:related jvr:-NT58TNXQ-G .

jvr:-W6ZT3KKJ-N
  skos:prefLabel "Trinucleotide Repeats"@en, "Répétitions de trinucléotides"@fr ;
  a mesh:Descriptor, skos:Concept ;
  skos:narrower jvr:-NT58TNXQ-G .