|
rdfs:label
|
"retinitis pigmentosa 19"@en
|
|
skos:altLabel
|
"RETINITIS PIGMENTOSA 19"@en
|
|
"RETINITIS PIGMENTOSA 19; RP19"@en
|
|
"RP 19"@en
|
|
"RP19"@en
|
|
"retinitis pigmentosa type 19"@en
|
|
schema:description
|
"Krankheit"@de
"retinitis pigmentosa that has material basis in mutation in the ABCA4 gene on chromosome 1p22"@en
"хвороба"@uk
"مرض يصيب الإنسان"@ar
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|
schema:dateModified
|
"2026-07-05T11:03:56+00:00"^^xsd:dateTime
|
|
schema:version
|
2514101662
|
|
wikibase:identifiers
|
8
|
|
wikibase:sitelinks
|
0
|
|
wikibase:statements
|
17
|
|
p:P11430
|
wd:statement/Q27677754-438c9bad-42de-cef2-fcbf-ba1fe85a167b
|
|
p:P2293
|
wd:statement/Q27677754-33A492A5-8128-4A04-9CBE-DB94758F5F78
|
|
p:P279
|
wd:statement/Q27677754-417A206F-A4EE-4938-BA5A-E28EC3032B10
|
|
wd:statement/Q27677754-501D75F2-6E2C-48BD-8DF0-237C43320C41
|
|
wd:statement/Q27677754-D2984FA3-860F-42F9-B807-89FADF9119AC
|
|
p:P2888
|
wd:statement/Q27677754-2C0B781B-DD15-4A2F-B5DE-55699E085194
|
|
wd:statement/Q27677754-B0390575-486E-4A3B-A0D4-96F0BD190ACE
|
|
p:P2892
|
wd:statement/Q27677754-62864D25-8251-46B9-A88E-1CE559833EF8
|
|
p:P31
|
wd:statement/Q27677754-7FCCDEE9-BCEE-432F-BA10-7042A54690FE
|
|
wd:statement/Q27677754-B2FB9EA3-00A9-4B02-B295-3024FBAD9B21
|
|
p:P4229
|
wd:statement/Q27677754-3E455126-589B-41E9-8775-5EAEA4E07CFF
|
|
p:P4317
|
wd:statement/Q27677754-93EA5B5C-9D5E-43FB-B8D3-667F23A77368
|
|
p:P486
|
wd:statement/Q27677754-2FC7912C-2617-4CBC-9796-05C5A9EA144B
|
|
p:P492
|
wd:statement/Q27677754-DB8EEB07-52C5-4665-B336-F56C2221625C
|
|
p:P5008
|
wd:statement/Q27677754-1BEC1076-07C0-4B5C-9B31-3279717F01E2
|
|
p:P5270
|
wd:statement/Q27677754-8C2E1B9B-87AD-4099-AE42-0A8D3918D47B
|
|
p:P699
|
wd:statement/Q27677754-14F475B6-0703-4AD6-8439-AAA311B35AE2
|
|
p:direct-normalized/P486
|
<http://id.nlm.nih.gov/mesh/C566637>
|
|
p:direct-normalized/P5270
|
<http://purl.obolibrary.org/obo/MONDO_0011137>
|
|
p:direct-normalized/P699
|
<http://purl.obolibrary.org/obo/DOID_DOID:0110354>
|
|
wdt:P11430
|
"DI-00985"
|
|
wdt:P2293
|
ABCA4
|
|
wdt:P279
|
autosomal recessive disease
|
|
retinitis pigmentosa
|
|
wdt:P2888
|
<http://identifiers.org/doid/DOID:0110354>
|
|
<http://purl.obolibrary.org/obo/DOID_0110354>
|
|
wdt:P2892
|
"C1866422"
|
|
wdt:P31
|
type of disease
|
|
rare disease
|
|
wdt:P4229
|
"H35.5"
|
|
wdt:P4317
|
"10398"
|
|
wdt:P486
|
"C566637"
|
|
wdt:P492
|
"601718"
|
|
wdt:P5008
|
WikiProject Medicine
|
|
wdt:P5270
|
"MONDO_0011137"
|
|
wdt:P699
|
"DOID:0110354"
|