|
rdfs:label
|
"retinitis pigmentosa 18"@en
|
|
skos:altLabel
|
"RETINITIS PIGMENTOSA 18"@en
|
|
"RETINITIS PIGMENTOSA 18; RP18"@en
|
|
"RP 18"@en
|
|
"RP18"@en
|
|
"Retinitis Pigmentosa type 18"@en
|
|
schema:description
|
"Krankheit"@de
"retinitis pigmentosa that has material basis in mutation in the PRPF3 gene on chromosome 1q21"@en
"хвороба"@uk
"مرض يصيب الإنسان"@ar
|
|
schema:dateModified
|
"2026-07-05T10:59:47+00:00"^^xsd:dateTime
|
|
schema:version
|
2514100452
|
|
wikibase:identifiers
|
8
|
|
wikibase:sitelinks
|
0
|
|
wikibase:statements
|
17
|
|
p:P11430
|
wd:statement/Q27677756-b8797440-4fbc-9de4-eb1e-caab5e2f1054
|
|
p:P2293
|
wd:statement/Q27677756-8A642154-FBFD-46B3-A60B-6C7E52F075D4
|
|
p:P279
|
wd:statement/Q27677756-1483BE3C-87E6-4009-8F66-96B9BF881759
|
|
wd:statement/Q27677756-596E57DA-C5DA-4B86-947D-467EC2DC8754
|
|
wd:statement/Q27677756-A5D28AE4-EAB1-408E-9211-9A548D1758FC
|
|
p:P2888
|
wd:statement/Q27677756-94D6DA16-BDB9-4BBC-9F3A-AED3F467279C
|
|
wd:statement/Q27677756-A467561D-4F3A-4F8A-A38C-2D77898780E5
|
|
p:P2892
|
wd:statement/Q27677756-67C3BEB2-EC1E-4B4F-AA64-89C49C69148F
|
|
p:P31
|
wd:statement/Q27677756-B0FF5B2B-C327-4B30-BA10-90E2C0CFFC90
|
|
wd:statement/Q27677756-BA903DB4-E72A-4051-B7EF-6BDAFB51BCA3
|
|
p:P4229
|
wd:statement/Q27677756-CA470F0C-8992-4080-891F-E569ADC3D85A
|
|
p:P4317
|
wd:statement/Q27677756-F919487B-7F6B-4120-BC42-EA48EDEE4D67
|
|
p:P486
|
wd:statement/Q27677756-6D3B6CD2-0A86-4579-9DFE-EDC38537CB66
|
|
p:P492
|
wd:statement/Q27677756-8A999EE5-E5C9-41B4-A4AF-76BD32EE4D82
|
|
p:P5008
|
wd:statement/Q27677756-E801CD16-3741-4445-9F4B-6C93878D2D51
|
|
p:P5270
|
wd:statement/Q27677756-67407560-7610-4FE6-8877-5BCA77F08D66
|
|
p:P699
|
wd:statement/Q27677756-5284CBFA-1338-430A-85DF-3E01F2B366C2
|
|
p:direct-normalized/P486
|
<http://id.nlm.nih.gov/mesh/C563320>
|
|
p:direct-normalized/P5270
|
<http://purl.obolibrary.org/obo/MONDO_0011075>
|
|
p:direct-normalized/P699
|
<http://purl.obolibrary.org/obo/DOID_DOID:0110356>
|
|
wdt:P11430
|
"DI-00984"
|
|
wdt:P2293
|
PRPF3
|
|
wdt:P279
|
autosomal dominant disease
|
|
retinitis pigmentosa
|
|
wdt:P2888
|
<http://identifiers.org/doid/DOID:0110356>
|
|
<http://purl.obolibrary.org/obo/DOID_0110356>
|
|
wdt:P2892
|
"C1832378"
|
|
wdt:P31
|
type of disease
|
|
rare disease
|
|
wdt:P4229
|
"H35.5"
|
|
wdt:P4317
|
"10392"
|
|
wdt:P486
|
"C563320"
|
|
wdt:P492
|
"601414"
|
|
wdt:P5008
|
WikiProject Medicine
|
|
wdt:P5270
|
"MONDO_0011075"
|
|
wdt:P699
|
"DOID:0110356"
|