@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 owl: <http://www.w3.org/2002/07/owl#> .
@prefix dc: <http://purl.org/dc/terms/> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .

jvr:-WWJHCQRB-K
  skos:prefLabel "surgery (Qualifier)"@en, "chirurgie (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-SDXQ5280-F
  skos:prefLabel "mortality (Qualifier)"@en, "mortalité (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-HPKB70N8-W
  skos:prefLabel "rehabilitation (Qualifier)"@en, "rééducation et réadaptation (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-VG20R78F-K
  skos:prefLabel "embryologie (Qualificatif)"@fr, "embryology (Qualifier)"@en ;
  a mesh:Qualifier, skos:Concept .

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

jvr:-L6C0XPHT-4
  skos:prefLabel "métabolisme (Qualificatif)"@fr, "metabolism (Qualifier)"@en ;
  a mesh:Qualifier, skos:Concept .

jvr:-WQ00QWRG-J
  skos:prefLabel "physiopathologie (Qualificatif)"@fr, "physiopathology (Qualifier)"@en ;
  a mesh:Qualifier, skos:Concept .

jvr:-DH7H9MJ2-N
  skos:prefLabel "anatomopathologie (Qualificatif)"@fr, "pathology (Qualifier)"@en ;
  a mesh:Qualifier, skos:Concept .

jvr:-MDQBX560-1
  skos:prefLabel "radiotherapy (Qualifier)"@en, "radiothérapie (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-ZJBZVRWR-8
  skos:prefLabel "parasitologie (Qualificatif)"@fr, "parasitology (Qualifier)"@en ;
  a mesh:Qualifier, skos:Concept .

jvr:-W6T67RP3-2
  skos:prefLabel "diagnostic imaging (Qualifier)"@en, "imagerie diagnostique (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-B6C87218-T
  skos:prefLabel "prévention et contrôle (Qualificatif)"@fr, "prevention & control (Qualifier)"@en ;
  a mesh:Qualifier, skos:Concept .

jvr:-BQ3W1P91-F
  skos:prefLabel "thérapie (Qualificatif)"@fr, "therapy (Qualifier)"@en ;
  a mesh:Qualifier, skos:Concept .

jvr:-KRXG97RR-5
  skos:prefLabel "diagnostic (Qualificatif)"@fr, "diagnosis (Qualifier)"@en ;
  a mesh:Qualifier, skos:Concept .

jvr:-JXB87Q1F-Q
  skos:prefLabel "Maladies neurodégénératives héréditaires"@fr, "Heredodegenerative Disorders, Nervous System"@en ;
  a mesh:Descriptor, skos:Concept ;
  skos:narrower jvr:-DWT3Q63S-2 .

jvr:-RM0ZQL2W-T
  skos:prefLabel "Spastic Paraplegia, Hereditary"@en, "Paraplégie spasmodique héréditaire"@fr ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-DWT3Q63S-2 .

jvr:-J9Z93VFN-9
  skos:prefLabel "enzymology (Qualifier)"@en, "enzymologie (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-T1QJHLQ4-J
  skos:prefLabel "microbiology (Qualifier)"@en, "microbiologie (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-MHKLJX03-S
  skos:prefLabel "Refsum Disease"@en, "Maladie de Refsum"@fr ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-DWT3Q63S-2 .

jvr:-KFM33PF8-L
  skos:prefLabel "médecine vétérinaire (Qualificatif)"@fr, "veterinary (Qualifier)"@en ;
  a mesh:Qualifier, skos:Concept .

jvr: a skos:ConceptScheme .
jvr:-KWV7RLT2-P
  skos:prefLabel "Malformations du système nerveux"@fr, "Nervous System Malformations"@en ;
  a mesh:Descriptor, skos:Concept ;
  skos:narrower jvr:-DWT3Q63S-2 .

jvr:-BBD0S71C-R
  skos:prefLabel "induit chimiquement (Qualificatif)"@fr, "chemically induced (Qualifier)"@en ;
  a mesh:Qualifier, skos:Concept .

jvr:-XVHTZRCG-7
  skos:prefLabel "étiologie (Qualificatif)"@fr, "etiology (Qualifier)"@en ;
  a mesh:Qualifier, skos:Concept .

jvr:-SDPG013V-D
  skos:prefLabel "psychology (Qualifier)"@en, "psychologie (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-P1X8SCQ6-K
  skos:prefLabel "virologie (Qualificatif)"@fr, "virology (Qualifier)"@en ;
  a mesh:Qualifier, skos:Concept .

jvr:-T6JZ48ZV-N
  skos:prefLabel "complications (Qualifier)"@en, "complications (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-W6SQV79N-S
  skos:prefLabel "classification (Qualifier)"@en, "classification (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-GXVR9QN8-P
  skos:prefLabel "drug therapy (Qualifier)"@en, "traitement médicamenteux (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-N8PXCD71-5
  skos:prefLabel "Syndrome d'Alström"@fr, "Alstrom Syndrome"@en ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-DWT3Q63S-2 .

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

jvr:-CB30NGKB-3
  skos:prefLabel "economics (Qualifier)"@en, "économie (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-HJN06C33-8
  skos:prefLabel "Maladie de Charcot-Marie-Tooth"@fr, "Charcot-Marie-Tooth Disease"@en ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-DWT3Q63S-2 .

jvr:-DWT3Q63S-2
  skos:altLabel "NHMS"@fr, "Neuropathie héréditaire sensitivomotrice"@fr, "NHMS (Neuropathie Héréditaire Motrice et Sensitive)"@fr, "Neuropathie sensitivo-motrice héréditaire"@fr, "Hereditary Motor and Sensory Neuropathies"@en, "NMSH"@fr, "NMSH (Neuropathie Motrice et Sensitive Héréditaire)"@fr, "HMSN"@en, "Neuropathie sensitivomotrice héréditaire"@fr, "Herditary Sensory and Motor Neuropathy"@en, "Neuropathie héréditaire sensitive et motrice"@fr, "Neuropathie héréditaire sensitivo-motrice"@fr, "Hereditary Motor and Sensory Neuropathy"@en, "Neuropathie motrice et sensorielle héréditaire"@fr, "Neuropathie héréditaire motrice et sensorielle"@fr, "Neuropathies, Hereditary Motor and Sensory"@en ;
  skos:broader jvr:-JXB87Q1F-Q, jvr:-KWV7RLT2-P, jvr:-MW8WSN0F-9 ;
  mesh:allowableQualifier jvr:-W4X1LN61-R, jvr:-KRXG97RR-5, jvr:-CSKTXWF5-F, jvr:-S0CS1X5R-5, jvr:-WQ00QWRG-J, jvr:-DH7H9MJ2-N, jvr:-VG20R78F-K, jvr:-NHL3D2X0-S, jvr:-WWJHCQRB-K, jvr:-T6JZ48ZV-N, jvr:-RC3PND0F-S, jvr:-XV06LPML-W, jvr:-SBNWSM1T-R, jvr:-HPKB70N8-W, jvr:-XVHTZRCG-7, jvr:-BT300B3G-Q, jvr:-T1QJHLQ4-J, jvr:-GXVR9QN8-P, jvr:-JVKFK2NX-2, jvr:-P1X8SCQ6-K, jvr:-L6C0XPHT-4, jvr:-SDXQ5280-F, jvr:-W6SQV79N-S, jvr:-BQ3W1P91-F, jvr:-W6T67RP3-2, jvr:-CB30NGKB-3, jvr:-J9Z93VFN-9, jvr:-SDPG013V-D, jvr:-Z9TSGBXH-4, jvr:-ZJBZVRWR-8, jvr:-B6C87218-T, jvr:-KFM33PF8-L, jvr:-MDQBX560-1, jvr:-BBD0S71C-R ;
  skos:hiddenLabel "NMSH de type 3"@fr, "NMSH de type III"@fr, "HMSN Type III"@en, "Neuropathie héréditaire motrice et sensitive de type VII"@fr, "NHMS de type 7"@fr, "Hereditary, Type VII, Motor and Sensory Neuropathy"@en, "Neuropathie héréditaire motrice et sensitive de type 7"@fr, "CMT4f"@en, "NHMS de type VII"@fr, "Hereditary Motor and Sensory Neuropathy Type III"@en, "Charcot-Marie-Tooth Disease, Demyelinating, Type 4f"@en, "NMSH de type VII"@fr, "Hereditary, Type III, Motor and Sensory Neuropathy"@en, "NHMS de type III"@fr, "Maladie de Déjerine-Sottas"@fr, "Dejerine-Sottas Syndrome"@en, "Dejerine-Sottas Disease"@en, "Neuropathie héréditaire motrice et sensorielle de type VII"@fr, "Neuropathie héréditaire motrice et sensitive de type 3"@fr, "HMSN3"@en, "Hereditary Motor and Sensory Neuropathy 3"@en, "Neuropathie motrice et sensitive héréditaire de type VII"@fr, "NMSH de type 7"@fr, "Hypertrophic Neuropathy of Dejerine-Sottas"@en, "Charcot-Marie-Tooth Disease, Type 3"@en, "Neuropathie motrice et sensitive héréditaire de type III"@fr, "Neuropathie héréditaire motrice et sensorielle de type III"@fr, "HMSN Type VII"@en, "NHMS de type 3"@fr, "Neuropathie héréditaire motrice et sensitive de type III"@fr, "Dejerine-Sottas Neuropathy"@en ;
  skos:prefLabel "Neuropathie héréditaire motrice et sensitive"@fr, "Hereditary Sensory and Motor Neuropathy"@en ;
  a skos:Concept, mesh:Descriptor ;
  skos:inScheme jvr: ;
  owl:sameAs <http://id.nlm.nih.gov/mesh/D015417> ;
  skos:narrower jvr:-P8C6TTVL-5, jvr:-RM0ZQL2W-T, jvr:-N8PXCD71-5, jvr:-HJN06C33-8, jvr:-MHKLJX03-S ;
  dc:modified "2018-06-30"^^xsd:date ;
  dc:established "1988-01-01"^^xsd:date ;
  skos:definition "A group of slowly progressive inherited disorders affecting motor and sensory peripheral nerves. Subtypes include HMSNs I-VII. HMSN I and II both refer to CHARCOT-MARIE-TOOTH DISEASE. HMSN III refers to hypertrophic neuropathy of infancy. HMSN IV refers to REFSUM DISEASE. HMSN V refers to a condition marked by a hereditary motor and sensory neuropathy associated with spastic paraplegia (see SPASTIC PARAPLEGIA, HEREDITARY). HMSN VI refers to HMSN associated with an inherited optic atrophy (OPTIC ATROPHIES, HEREDITARY), and HMSN VII refers to HMSN associated with retinitis pigmentosa. (From Adams et al., Principles of Neurology, 6th ed, p1343)"@en ;
  dc:created "1999-11-08"^^xsd:date .

jvr:-CSKTXWF5-F
  skos:prefLabel "epidemiology (Qualifier)"@en, "épidémiologie (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-BT300B3G-Q
  skos:prefLabel "cerebrospinal fluid (Qualifier)"@en, "liquide cérébrospinal (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-JVKFK2NX-2
  skos:prefLabel "nursing (Qualifier)"@en, "soins infirmiers (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-W4X1LN61-R
  skos:prefLabel "diet therapy (Qualifier)"@en, "diétothérapie (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-P8C6TTVL-5
  skos:prefLabel "Giant Axonal Neuropathy"@en, "Neuropathie à axones géants"@fr ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-DWT3Q63S-2 .

jvr:-MW8WSN0F-9
  skos:prefLabel "Polyneuropathies"@fr, "Polyneuropathies"@en ;
  a mesh:Descriptor, skos:Concept ;
  skos:narrower jvr:-DWT3Q63S-2 .

jvr:-RC3PND0F-S
  skos:prefLabel "ethnology (Qualifier)"@en, "ethnologie (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-XV06LPML-W
  skos:prefLabel "urine (Qualifier)"@en, "urine (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-NHL3D2X0-S
  skos:prefLabel "sang (Qualificatif)"@fr, "blood (Qualifier)"@en ;
  a mesh:Qualifier, skos:Concept .

jvr:-SBNWSM1T-R
  skos:prefLabel "history (Qualifier)"@en, "histoire (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

