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Namespace Prefixes

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wdshttp://www.wikidata.org/entity/statement/
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Statements

Subject Item
wd:Q1531333
rdf:type
wikibase:Item
schema:description
autosomal recessive limb-girdle muscular dystrophy that has material basis in mutation in the gene encoding telethonin (TCAP) مرض يصيب الإنسان Krankheit хвороба
p:P2888
wds:Q1531333-FF1BB5A8-3235-44A0-B9BD-50166776BD68 wds:Q1531333-CB4E2C26-2411-4E33-B3B9-CC4D1E530566 wds:Q1531333-A51C5A98-5C06-48EA-8B27-F07C8C18172C
wdt:P2888
n8:DOID_0110281 n14:Orphanet_34514 n15:0110281
p:P1995
wds:Q1531333-30B0903C-B9EF-49BF-A016-1F17985BF571
p:P5270
wds:Q1531333-0C8BEC8F-3210-4C6D-A640-E20093480DE9
p:P699
wds:Q1531333-62F1BB6B-B47C-4CFC-9B0A-F5EFE0DAAB74
wdtn:P5270
n8:MONDO_0011170
wdtn:P699
n12:0110281
wdt:P1995
wd:Q83042
wdt:P5270
MONDO_0011170
wdt:P699
DOID:0110281
rdfs:label
dystrophie musculaire des ceintures type 2G Gliedergürteldystrophie 2G autosomal recessive limb-girdle muscular dystrophy type 2G
skos:prefLabel
dystrophie musculaire des ceintures type 2G autosomal recessive limb-girdle muscular dystrophy type 2G Gliedergürteldystrophie 2G
schema:name
autosomal recessive limb-girdle muscular dystrophy type 2G dystrophie musculaire des ceintures type 2G Gliedergürteldystrophie 2G
p:P31
wds:Q1531333-916AE927-474E-44EA-9A8C-3853FB61C141 wds:Q1531333-8EBA68A0-F196-43C6-A98B-65DFB4608E2E
wdt:P31
wd:Q112193867 wd:Q929833
p:P279
wds:Q1531333-07B3C2AE-9411-426C-AD32-18C0EA87A943 wds:Q1531333-C5A8C208-361B-40C0-BC7A-13DBA6431F0C
wdt:P279
wd:Q27429766 wd:Q55786011
p:P1550
wds:Q1531333-BB97C5EF-5F36-43C2-9940-B954989468D0
p:P2293
wds:Q1531333-25BD5E6F-855A-490F-BAB2-124DA3C972C0
p:P4229
wds:Q1531333-F406A17C-5B5C-4ECC-90BB-368AC57E7367
p:P4317
wds:Q1531333-38E65D1B-FFFE-4F6F-8956-3371F9915509
p:P492
wds:Q1531333-05314612-BEA7-4546-91EC-6A74FFE7DC18
wdt:P1550
34514
wdt:P2293
wd:Q18033105
wdt:P4229
G71.0
wdt:P4317
10471
wdt:P492
601954
skos:altLabel
muscular dystrophy, limb-girdle, type 2G MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2G; LGMD2G Telethoninopathie limb-girdle muscular dystrophy due to telethonin deficiency LGMD2G LGMD2G
p:P2892
wds:Q1531333-98C9F5E9-D00A-42CD-AA11-7B38BE2784A6
p:P486
wds:Q1531333-9B7CF4B0-760F-4E79-86A3-33862B941B30
p:P5008
wds:Q1531333-C5F00B9B-C459-4C12-8124-E4F61816A874
wdtn:P486
n13:C566599
wdt:P2892
C1866008
wdt:P486
C566599
wdt:P5008
wd:Q4099686