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rdfs:label
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"5q-minus-Syndrom"@de
"5q-syndrom"@nn
"5q-症候群"@ja
"5號染色體長臂缺失症候群"@zh
"Sindrom delecije 5q"@bs
"Síndrome del 5q"@es
"Síndrome mielodisplásica associada a anomalia cromossômica 5q isolada"@pt
"Síndrome mielodisplásica associada a anomalia cromossômica 5q isolada"@pt-br
"chromosome 5q deletion syndrome"@en
"sindrom delecije kromosoma 5q"@sl
"syndrome 5q-"@fr
"sìndrome del 5q"@vec
"متلازمة حذف كروموسوم 5q"@ar
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skos:altLabel
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"5Q minus syndrome"@en
"5q- syndrome"@en
"5q- syndrome, refractory macrocytic anemia due to 5q deletion"@en
"CHROMOSOME 5q DELETION SYNDROME"@en
"Macrocytic Anemia, Refractory, Due to 5Q Deletion"@en
"Megakaryocytes, Unilobular Nucleated"@en
"Myelodysplastic Syndrome Associated with Isolated del (5q) Chromosome Abnormality"@en
"Myelodysplastic Syndrome with 5q Deletion"@en
"Myelodysplastic Syndrome with Isolated del(5q)"@en
"del(5q)"@nn
"delesjon 5q"@nn
"myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality"@en
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schema:description
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"forme de myélodysplasie causée par une délétion du chromosome 5"@fr
"human disease"@en
"malattia"@it
"myelodysplastisches Syndrom"@de
"хвороба людини"@uk
"մարդու հիվանդություն"@hy
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schema:dateModified
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"2026-10-24T00:39:43+00:00"^^xsd:dateTime
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schema:version
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2560167757
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wikibase:identifiers
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20
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22
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wikibase:sitelinks
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8
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wikibase:statements
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55
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p:P11143
|
wd:statement/Q245455-38B99A6F-F938-42EB-A5BE-7CB4D0430CDC
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p:P1193
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wd:statement/Q245455-4E246AD6-A58B-4D54-9164-0502ACD12B17
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p:P14914
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wd:statement/Q245455-466CAC51-F747-4AFC-B524-986046AEAC46
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p:P1550
|
wd:statement/Q245455-DA559214-FF04-443E-9A19-796EE0210CB5
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p:P1748
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wd:statement/Q245455-35CE34BC-B853-41DA-85A8-4E94D682B018
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p:P1995
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wd:statement/Q245455-ef7ece11-4d8e-4061-adf9-0980865ec14c
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p:P2176
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wd:statement/Q245455-B20A9351-795F-4C81-9E56-0D5D3D258D89
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p:P2293
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wd:statement/Q245455-30A73423-67C8-4435-8CA4-F40C5438B8C7
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p:P279
|
wd:statement/Q245455-1E191959-D617-4530-BBA6-F938494E3452
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|
wd:statement/Q245455-1F36E9A2-EBD8-4ACE-9A1A-4E89E8E8E247
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wd:statement/Q245455-5247C5C7-0F35-4FE9-BEA0-C54D8A408D2E
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wd:statement/Q245455-5d0cccde-431a-67fe-d701-0e96d0ac7428
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wd:statement/Q245455-B132690A-BCA1-41DF-BA43-68C1ABEA90DC
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wd:statement/Q245455-B84E2A83-7E41-41E3-8D3F-24CD7C64916D
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wd:statement/Q245455-BED0A1D7-EDCB-4EB7-842F-683AE63B2660
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wd:statement/Q245455-CDB02040-DCF3-4E37-BA52-E7209C62C5C6
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wd:statement/Q245455-DBEB0049-B04F-4BD0-B0AB-7888A8537CD0
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p:P2841
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wd:statement/Q245455-2D451A65-CA71-49BB-90AE-FBE90B895E84
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p:P2888
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wd:statement/Q245455-509A406C-6774-4F16-819E-472E79E74B79
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wd:statement/Q245455-63F29216-32CD-480D-B33D-220772699433
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wd:statement/Q245455-956123B1-B60E-4933-9096-1298F3A7CD65
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p:P2892
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wd:statement/Q245455-4BE0A9F2-C43D-4BBC-9906-26A09A1A99E8
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wd:statement/Q245455-69E22558-398A-4AF8-A726-55A38B463900
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wd:statement/Q245455-9CDDCF93-0FDD-4EB0-8BE3-522B63AB6C45
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p:P31
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wd:statement/Q245455-13B338B7-F157-4442-90CA-188846AAC9F0
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p:P373
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wd:statement/Q245455-a6502584-4d57-55fc-7c19-9a1d91e3eb8d
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p:P4229
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wd:statement/Q245455-C20A36B9-4E0B-47C2-8856-3A21D9683324
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p:P4317
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wd:statement/Q245455-87B8109E-5AE1-4516-9B7B-298AFB027003
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wd:statement/Q245455-9C9C8720-803C-4A69-882E-6CA3CC3F8317
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p:P486
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wd:statement/Q245455-4E1EE3B9-27BC-401F-89CC-38557E47E74B
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p:P492
|
wd:statement/Q245455-973EAD73-112F-4DE0-91D1-B87474B114C9
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p:P5008
|
wd:statement/Q245455-62A62FBD-D422-4A90-ABD3-102C53041143
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p:P5270
|
wd:statement/Q245455-0038E8D2-BAD0-4F7B-B140-3D734FBF6016
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p:P557
|
wd:statement/q245455-62BB509B-4681-46DB-BDAD-C36385EDA158
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p:P563
|
wd:statement/q245455-28300047-B3EE-4627-BF8E-5BF1969904C2
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p:P6366
|
wd:statement/Q245455-A2617ABD-D1F9-4953-9F5D-F09886B3B849
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p:P646
|
wd:statement/Q245455-8DB989FA-B316-4D13-8FDC-CACD94D905E0
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p:P6532
|
wd:statement/Q245455-109A583A-4E80-40EC-9C09-80D22CDEA30D
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|
wd:statement/Q245455-50F7D973-0597-4CBA-AF90-C2E5CB57E733
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wd:statement/Q245455-5E9DC3CB-8E81-4EB1-9F29-F9D12ACB794A
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wd:statement/Q245455-6598C1B7-FEFE-4BA0-A98F-2E780F5176DE
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wd:statement/Q245455-65D9173C-3875-4309-9247-CDE267DBC2E3
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wd:statement/Q245455-6C05E5E0-2DBE-438D-9156-ADE16989AA55
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wd:statement/Q245455-92181D21-1384-4E11-B643-77E8169E33C5
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wd:statement/Q245455-D6E98E3A-4983-4EBA-8A4A-03D352057BE0
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wd:statement/Q245455-DFFD8A5A-130F-43D2-B1D0-B8E8DB1AF6F7
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wd:statement/Q245455-E06125ED-463C-4386-9B91-ED9503E98CE6
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wd:statement/Q245455-E21891DB-6D3B-4FD5-89AD-D91572B5B67F
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wd:statement/Q245455-EBFEEDDA-A69F-4B0E-9A02-2C4E315BE352
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wd:statement/Q245455-FE4E5435-988C-43A1-A748-0F1B15983F2F
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p:P665
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wd:statement/Q245455-D160BE79-92ED-4E6B-856A-F118E9B15EE4
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p:P699
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wd:statement/Q245455-E67D4BB6-B19F-44F7-8B65-0279BD15B8AD
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p:P7329
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wd:statement/Q245455-C7A94CC7-29EA-4AD0-8685-C77EE41239A7
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p:P7464
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wd:statement/Q245455-EB8E6D71-A620-4E28-8053-A527A60F2E9F
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p:P7807
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wd:statement/Q245455-69C4545E-24C6-46E2-9FC7-FE0F0A9CD282
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p:direct-normalized/P486
|
<http://id.nlm.nih.gov/mesh/C535323>
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p:direct-normalized/P5270
|
<http://purl.obolibrary.org/obo/MONDO_0007925>
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|
p:direct-normalized/P6366
|
<https://makg.org/entity/2779004087>
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p:direct-normalized/P665
|
<http://www.kegg.jp/entry/H01484>
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p:direct-normalized/P699
|
<http://purl.obolibrary.org/obo/DOID_DOID:0090016>
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|
wdt:P11143
|
"Chromosome 5q deletion syndrome"
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|
wdt:P1193
|
0.000001^^xsd:decimal
|
|
wdt:P14914
|
"D86841"
|
|
wdt:P1550
|
"86841"
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|
wdt:P1748
|
"C6867"
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wdt:P1995
|
hematology
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wdt:P2176
|
(RS)-lenalidomide
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wdt:P2293
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RPS14
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wdt:P279
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hereditary neoplastic syndromes
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chromosomal deletion syndrome
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congenital anemia
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macrocytic anemia
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|
inherited syndrome with bone tumors as a major feature
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rare genetic immune disease
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partial deletion of the long arm of chromosome 5
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myelodysplastic syndrome
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wdt:P2841
|
adult onset
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wdt:P2888
|
<http://identifiers.org/doid/DOID:0090016>
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|
<http://purl.obolibrary.org/obo/DOID_0090016>
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|
<http://www.orpha.net/ORDO/Orphanet_86841>
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|
wdt:P2892
|
"C0740302"
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|
"C1292779"
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|
"C1835193"
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|
wdt:P31
|
type of disease
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|
wdt:P373
|
"Chromosome 5q deletion syndrome"
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|
wdt:P4229
|
"D46.7"
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|
wdt:P4317
|
"10840"
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|
"8723"
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|
wdt:P486
|
"C535323"
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|
wdt:P492
|
"153550"
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|
wdt:P5008
|
WikiProject Medicine
|
|
wdt:P5270
|
"MONDO_0007925"
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|
wdt:P557
|
"34573"
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|
wdt:P563
|
"9986/3"
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|
wdt:P6366
|
"2779004087"
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|
wdt:P646
|
"/m/04r3cv"
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|
wdt:P6532
|
persistent infection
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|
Abnormal bleeding
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Abnormal neutrophil morphology
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Abnormality of bone marrow stromal cells
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Abnormal megakaryocyte morphology
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Multiple lineage myelodysplasia
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thrombogavitis
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macrocytic anemia
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acute myeloid leukemia
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leukopenia
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bone marrow failure
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anisocytosis
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myelodysplastic syndrome
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wdt:P665
|
"H01484"
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|
wdt:P699
|
"DOID:0090016"
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|
wdt:P7329
|
"2A36"
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|
wdt:P7464
|
"5q-minus-syndrome"
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|
wdt:P7807
|
"420472577"
|