|
rdfs:label
|
"retinitis pigmentosa 12"@en
|
|
skos:altLabel
|
"RETINITIS PIGMENTOSA 12"@en
|
|
"RETINITIS PIGMENTOSA 12; RP12"@en
|
|
"RP 12"@en
|
|
"RP12"@en
|
|
"Retinitis Pigmentosa With or Without Paraarteriolar Preservation of Retinal Pigment Epithelium"@en
|
|
"Retinitis Pigmentosa type 12"@en
|
|
"Rp With or Without Pprpe"@en
|
|
"Rp With or Without Preserved Paraarteriole Retinal Pigment Epithelium"@en
|
|
schema:description
|
"Krankheit"@de
"retinitis pigmentosa that has material basis in mutation in the CRB1 gene on chromosome 1q31.3"@en
"хвороба"@uk
"مرض يصيب الإنسان"@ar
|
|
schema:dateModified
|
"2026-07-05T11:03:55+00:00"^^xsd:dateTime
|
|
schema:version
|
2514101659
|
|
wikibase:identifiers
|
8
|
|
wikibase:sitelinks
|
0
|
|
wikibase:statements
|
17
|
|
p:P11430
|
wd:statement/Q27677758-435d892f-4ad2-59ba-85a5-a51ddb7c9f32
|
|
p:P2293
|
wd:statement/Q27677758-9D7ED79C-CB83-4E64-A05E-16EFFF0E1986
|
|
p:P279
|
wd:statement/Q27677758-E59E3713-62EF-4A48-9986-F4AD63C408DC
|
|
wd:statement/Q27677758-ECC516AB-BFBF-41C4-9F2C-A2092062A070
|
|
wd:statement/Q27677758-FFB380CC-36B8-48F3-A9C6-0DF65D578E43
|
|
p:P2888
|
wd:statement/Q27677758-1DD84879-2BB7-498D-ADF5-4F980A74396A
|
|
wd:statement/Q27677758-3ECC7771-E836-4C6B-B102-0CB39E0191AE
|
|
p:P2892
|
wd:statement/Q27677758-F7A85433-AC19-4875-A397-859E318EEDD2
|
|
p:P31
|
wd:statement/Q27677758-60740DFD-5A7D-4E1D-98A5-3A2E99E94738
|
|
wd:statement/Q27677758-EAC8F9D4-EB3E-4FB4-9806-E6C80B7F5730
|
|
p:P4229
|
wd:statement/Q27677758-AA8565E6-42B5-47ED-AA71-E16A77208710
|
|
p:P4317
|
wd:statement/Q27677758-FB6B40E9-42C1-4DA6-9770-ED9BC896147B
|
|
p:P486
|
wd:statement/Q27677758-19C6E4B9-FB6F-456D-AB57-314F7C21DD2A
|
|
p:P492
|
wd:statement/Q27677758-4314C269-2C5C-4CEB-AA31-01699D813B1C
|
|
p:P5008
|
wd:statement/Q27677758-1DA46424-4431-4DB7-A054-7C2D3EE8AF16
|
|
p:P5270
|
wd:statement/Q27677758-68079305-EE37-4E3F-AD66-241E42AA6E76
|
|
p:P699
|
wd:statement/Q27677758-A9B93F20-8779-4B12-98DD-618CDBF7910E
|
|
p:direct-normalized/P486
|
<http://id.nlm.nih.gov/mesh/C563999>
|
|
p:direct-normalized/P5270
|
<http://purl.obolibrary.org/obo/MONDO_0010818>
|
|
p:direct-normalized/P699
|
<http://purl.obolibrary.org/obo/DOID_DOID:0110358>
|
|
wdt:P11430
|
"DI-00979"
|
|
wdt:P2293
|
CRB1
|
|
wdt:P279
|
autosomal recessive disease
|
|
retinitis pigmentosa
|
|
wdt:P2888
|
<http://identifiers.org/doid/DOID:0110358>
|
|
<http://purl.obolibrary.org/obo/DOID_0110358>
|
|
wdt:P2892
|
"C1838647"
|
|
wdt:P31
|
type of disease
|
|
rare disease
|
|
wdt:P4229
|
"H35.5"
|
|
wdt:P4317
|
"10376"
|
|
wdt:P486
|
"C563999"
|
|
wdt:P492
|
"600105"
|
|
wdt:P5008
|
WikiProject Medicine
|
|
wdt:P5270
|
"MONDO_0010818"
|
|
wdt:P699
|
"DOID:0110358"
|