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rdfs:label
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"Hereditary CNS demyelinating disease"@en
"demyeliniserande sjukdom i sentralnervesystemet, arveleg"@nn
"maladies démyélinisantes héréditaires du système nerveux central"@fr
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skos:altLabel
|
"arveleg demyeliniserande sjukdom i sentralnervesystemet"@nn
"demyeliniserande sjukdom i sentralnervesystemet, hereditær"@nn
"hereditary central nervous system demyelinating disease"@en
"hereditær"@nn
"obsolete hereditary central nervous system demyelinating disease"@en
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schema:description
|
"Human disease"@en
"Krankheit"@de
"malattia"@it
"хвороба людини"@uk
"մարդու հիվանդություն"@hy
"مرض يصيب الإنسان"@ar
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schema:dateModified
|
"2026-07-04T14:21:56+00:00"^^xsd:dateTime
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schema:version
|
2513829394
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wikibase:identifiers
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12
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wikibase:sitelinks
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1
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wikibase:statements
|
21
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p:P1995
|
wd:statement/Q17048613-4C507A06-2C9E-4093-BF9C-10BA307F8DCB
|
|
wd:statement/Q17048613-53F91D3B-0EB7-4B0B-94C5-BFECEE7E55D1
|
|
wd:statement/Q17048613-C65631B4-04AF-40D4-BD52-600F71B21F64
|
|
p:P279
|
wd:statement/Q17048613-faac00a1-476c-a67f-48e2-bf3a5c15066e
|
|
wd:statement/Q17048613-fdbc7452-4bda-cb8e-3da8-cd39baeb5757
|
|
p:P2888
|
wd:statement/Q17048613-7DE92F62-F986-49AA-9CBB-142F284914B9
|
|
wd:statement/Q17048613-E70FEBFE-24D7-4934-9970-6A7E181B0C86
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|
p:P2892
|
wd:statement/Q17048613-234D03B8-09E0-4112-9EE8-4D5A48917AC8
|
|
p:P31
|
wd:statement/Q17048613-56F1D36C-F090-43E8-8B2F-64258A5E4874
|
|
p:P486
|
wd:statement/Q17048613-f44353eb-429d-3cba-5d34-124aafc1383a
|
|
p:P5008
|
wd:statement/Q17048613-0EC6B55B-1009-4F3A-86A7-FF34195D883F
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|
p:P6366
|
wd:statement/Q17048613-CD98E12E-AA70-4AC4-A5CA-015CB2D27CAB
|
|
p:P672
|
wd:statement/Q17048613-24022772-2251-40FB-9142-E5FBDB93E528
|
|
wd:statement/Q17048613-275AEECD-FD20-4689-8239-7DC86014C2AA
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|
wd:statement/Q17048613-27612727-A3B3-446F-9985-533FFCC0BBF2
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|
wd:statement/Q17048613-4EB6BC00-1F23-4218-9E6C-A402DDD1CBE5
|
|
wd:statement/Q17048613-6944e0f9-4dec-1a55-465e-3c611e61d0fa
|
|
wd:statement/Q17048613-C1D496E4-F327-43C5-81E8-A1DDF1564B0A
|
|
wd:statement/Q17048613-D131DE52-A014-4FD6-BCB3-4EDE41C65F93
|
|
wd:statement/Q17048613-E964DA37-1EFF-4E74-947B-6A4DA287A358
|
|
p:P699
|
wd:statement/Q17048613-E55157DF-2AF3-4997-8F61-B68BBFBDCAC5
|
|
p:direct-normalized/P486
|
<http://id.nlm.nih.gov/mesh/D020279>
|
|
p:direct-normalized/P6366
|
<https://makg.org/entity/2909832350>
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|
p:direct-normalized/P672
|
<http://id.nlm.nih.gov/mesh/C10.228.140.163.100.362>
|
|
<http://id.nlm.nih.gov/mesh/C10.228.140.695.625>
|
|
<http://id.nlm.nih.gov/mesh/C10.314.400>
|
|
<http://id.nlm.nih.gov/mesh/C10.574.500.490>
|
|
<http://id.nlm.nih.gov/mesh/C16.320.400.367>
|
|
<http://id.nlm.nih.gov/mesh/C16.320.565.189.362>
|
|
<http://id.nlm.nih.gov/mesh/C18.452.132.100.362>
|
|
<http://id.nlm.nih.gov/mesh/C18.452.648.189.362>
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wdt:P1995
|
medical genetics
|
|
endocrinology
|
|
neurology
|
|
wdt:P279
|
demyelinating disease of central nervous system
|
|
hereditary disorder
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|
wdt:P2892
|
"C0751877"
|
|
wdt:P31
|
type of disease
|
|
wdt:P486
|
"D020279"
|
|
wdt:P5008
|
WikiProject Medicine
|
|
wdt:P6366
|
"2909832350"
|
|
wdt:P672
|
"C10.228.140.163.100.362"
|
|
"C10.228.140.695.625"
|
|
"C10.314.400"
|
|
"C10.574.500.490"
|
|
"C16.320.400.367"
|
|
"C16.320.565.189.362"
|
|
"C18.452.132.100.362"
|
|
"C18.452.648.189.362"
|