@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:-MLD02K7C-B
  skos:prefLabel "Expansion de séquence répétée de l'ADN"@fr, "DNA Repeat Expansion"@en ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-Z5N478GX-B .

jvr:-C5JDW1L3-L
  skos:prefLabel "Mutation, Missense"@en, "Mutation faux-sens"@fr ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-Z5N478GX-B .

jvr:-HCDN5Q0B-0
  skos:prefLabel "Accumulation de mutations"@fr, "Mutation Accumulation"@en ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-Z5N478GX-B .

jvr:-MSFRFH4H-P
  skos:prefLabel "Base Pair Mismatch"@en, "Mésappariement de bases"@fr ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-Z5N478GX-B .

jvr:-VGN1N1M3-P
  skos:prefLabel "Point Mutation"@en, "Mutation ponctuelle"@fr ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-Z5N478GX-B .

jvr:-BX4GVVNJ-X
  skos:prefLabel "Sequence Deletion"@en, "Délétion de séquence"@fr ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-Z5N478GX-B .

jvr:-X53PRGP1-5
  skos:prefLabel "Amplification de gène"@fr, "Gene Amplification"@en ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-Z5N478GX-B .

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

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:-WN4NR7JK-S
  skos:prefLabel "Mutagenesis, Insertional"@en, "Mutagenèse par insertion"@fr ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-Z5N478GX-B .

jvr:-RQM0BSS4-8
  skos:prefLabel "Chromosome Aberrations"@en, "Aberrations des chromosomes"@fr ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-Z5N478GX-B .

jvr:-Z69CL4G0-S
  skos:prefLabel "Mutation de type INDEL"@fr, "INDEL Mutation"@en ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-Z5N478GX-B .

jvr:-VPP2JF3W-S
  skos:prefLabel "Gain of Function Mutation"@en, "Mutation gain de fonction"@fr ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-Z5N478GX-B .

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

jvr:-WG4VH552-W
  skos:prefLabel "Mutation avec décalage du cadre de lecture"@fr, "Frameshift Mutation"@en ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-Z5N478GX-B .

jvr: a skos:ConceptScheme .
jvr:-VD99PWBW-6
  skos:prefLabel "Suppression génétique"@fr, "Suppression, Genetic"@en ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-Z5N478GX-B .

jvr:-C0K9WRPB-X
  skos:prefLabel "Mutagenèse"@fr, "Mutagenesis"@en ;
  a mesh:Descriptor, skos:Concept ;
  skos:related jvr:-Z5N478GX-B .

jvr:-GM3G5SW3-M
  skos:prefLabel "DNA Damage"@en, "Altération de l'ADN"@fr ;
  a mesh:Descriptor, skos:Concept ;
  skos:related jvr:-Z5N478GX-B .

jvr:-S2FN6N83-K
  skos:prefLabel "Mutagens"@en, "Mutagènes"@fr ;
  a mesh:Descriptor, skos:Concept ;
  skos:related jvr:-Z5N478GX-B .

jvr:-NFTCFT64-4
  skos:prefLabel "Allelic Imbalance"@en, "Déséquilibre allélique"@fr ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-Z5N478GX-B .

jvr:-DGHPGRM8-4
  skos:prefLabel "Inversion de séquence"@fr, "Sequence Inversion"@en ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-Z5N478GX-B .

jvr:-F8XVJHT2-8
  skos:prefLabel "Mutation germinale"@fr, "Germ-Line Mutation"@en ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-Z5N478GX-B .

jvr:-WHLR0VL7-1
  skos:prefLabel "Antimutagenic Agents"@en, "Antimutagènes"@fr ;
  a mesh:Descriptor, skos:Concept ;
  skos:related jvr:-Z5N478GX-B .

jvr:-LMSM97MB-S
  skos:prefLabel "Mutation inapparente"@fr, "Silent Mutation"@en ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-Z5N478GX-B .

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

jvr:-Z5N478GX-B
  skos:inScheme jvr: ;
  skos:related jvr:-S2FN6N83-K, jvr:-GM3G5SW3-M, jvr:-NGBS5G2J-5, jvr:-WHLR0VL7-1, jvr:-C0K9WRPB-X ;
  mesh:allowableQualifier jvr:-H7K65Q8S-Z, jvr:-WZF2ZR3L-B, jvr:-PPKJKFKK-V, jvr:-S0CS1X5R-5, jvr:-N2WP45CN-V, jvr:-Z9TSGBXH-4 ;
  skos:narrower jvr:-C5JDW1L3-L, jvr:-NFTCFT64-4, jvr:-WN4NR7JK-S, jvr:-VPP2JF3W-S, jvr:-Z69CL4G0-S, jvr:-WQQ1W1SB-N, jvr:-HCDN5Q0B-0, jvr:-N47TCCKD-5, jvr:-VGN1N1M3-P, jvr:-X53PRGP1-5, jvr:-MSFRFH4H-P, jvr:-F8XVJHT2-8, jvr:-WG4VH552-W, jvr:-QGH2Z0TX-K, jvr:-TZS96GKK-N, jvr:-RQM0BSS4-8, jvr:-MLD02K7C-B, jvr:-BVRZ78N7-J, jvr:-T739CM7H-2, jvr:-LMSM97MB-S, jvr:-DGHPGRM8-4, jvr:-VD99PWBW-6, jvr:-BX4GVVNJ-X ;
  dc:created "1999-01-01"^^xsd:date ;
  owl:sameAs <http://id.nlm.nih.gov/mesh/D009154> ;
  a skos:Concept, mesh:Descriptor ;
  skos:prefLabel "Mutation"@en, "Mutation"@fr ;
  skos:broader jvr:-B5CT14VJ-D ;
  dc:established "1964-01-01"^^xsd:date ;
  dc:modified "2008-07-08"^^xsd:date ;
  skos:definition "Any detectable and heritable change in the genetic material that causes a change in the GENOTYPE and which is transmitted to daughter cells and to succeeding generations."@en .

jvr:-N47TCCKD-5
  skos:prefLabel "Mutation perte de fonction"@fr, "Loss of Function Mutation"@en ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-Z5N478GX-B .

jvr:-TZS96GKK-N
  skos:prefLabel "Genomic Instability"@en, "Instabilité du génome"@fr ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-Z5N478GX-B .

jvr:-NGBS5G2J-5
  skos:prefLabel "Polymorphisme de restriction"@fr, "Polymorphism, Restriction Fragment Length"@en ;
  a mesh:Descriptor, skos:Concept ;
  skos:related jvr:-Z5N478GX-B .

jvr:-B5CT14VJ-D
  skos:prefLabel "Genetic Variation"@en, "Variation génétique"@fr ;
  a mesh:Descriptor, skos:Concept ;
  skos:narrower jvr:-Z5N478GX-B .

jvr:-WQQ1W1SB-N
  skos:prefLabel "Gene Duplication"@en, "Duplication de gène"@fr ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-Z5N478GX-B .

jvr:-QGH2Z0TX-K
  skos:prefLabel "Taux de mutation"@fr, "Mutation Rate"@en ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-Z5N478GX-B .

jvr:-T739CM7H-2
  skos:prefLabel "Codon non-sens"@fr, "Codon, Nonsense"@en ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-Z5N478GX-B .

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

jvr:-BVRZ78N7-J
  skos:prefLabel "Mutations synthétiques létales"@fr, "Synthetic Lethal Mutations"@en ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-Z5N478GX-B .