|
rdfs:label
|
"retinitis pigmentosa 42"@en
|
|
skos:altLabel
|
"RETINITIS PIGMENTOSA 42"@en
|
|
"RETINITIS PIGMENTOSA 42; RP42"@en
|
|
"RP42"@en
|
|
"Retinitis Pigmentosa type 42"@en
|
|
schema:description
|
"Krankheit"@de
"retinitis pigmentosa that has material basis in mutation in the KLHL7 gene on chromosome 7p15.3"@en
"хвороба"@uk
"مرض يصيب الإنسان"@ar
|
|
schema:dateModified
|
"2026-07-05T10:59:45+00:00"^^xsd:dateTime
|
|
schema:version
|
2514100439
|
|
wikibase:identifiers
|
7
|
|
wikibase:sitelinks
|
0
|
|
wikibase:statements
|
16
|
|
p:P11430
|
wd:statement/Q27677785-27a14644-413b-df83-0b32-5cbfa135315c
|
|
p:P2293
|
wd:statement/Q27677785-615093F8-2273-4CD8-BE7B-5BD106449797
|
|
p:P279
|
wd:statement/Q27677785-3FEDE6AE-9593-4E92-81EB-221E0C368FB9
|
|
wd:statement/Q27677785-C0B55EE3-4231-4425-A506-7AE98111F900
|
|
wd:statement/Q27677785-EC7B98CA-65FD-4A69-8A46-F4C4A6280E61
|
|
p:P2888
|
wd:statement/Q27677785-3285EA70-3BF6-4178-A72B-8CEA70836556
|
|
wd:statement/Q27677785-78998319-017A-44F7-BDBB-54B2B6E6C89A
|
|
p:P2892
|
wd:statement/Q27677785-3780EAF9-2321-4FD6-B2EE-AF38DDA77B1D
|
|
p:P31
|
wd:statement/Q27677785-49E147D6-AED3-4ED4-9475-77558E464FE0
|
|
wd:statement/Q27677785-68BCA0F8-1177-49AB-AA86-47E6ACDA72AA
|
|
p:P4229
|
wd:statement/Q27677785-F64C3557-6C7E-4582-B3BE-6C7A01E80598
|
|
p:P486
|
wd:statement/Q27677785-38E54065-F9D0-40D3-B3DE-D7A563D89615
|
|
p:P492
|
wd:statement/Q27677785-3B18F2DB-7109-493E-9BD5-9C09EE1D55DD
|
|
p:P5008
|
wd:statement/Q27677785-1C148C39-087B-4CDE-9579-FADB2569B5A3
|
|
p:P5270
|
wd:statement/Q27677785-EABC478D-592D-465A-980A-E7A6B89CF637
|
|
p:P699
|
wd:statement/Q27677785-5DFDD623-F1E1-4679-A640-645C8961C65D
|
|
p:direct-normalized/P486
|
<http://id.nlm.nih.gov/mesh/C567854>
|
|
p:direct-normalized/P5270
|
<http://purl.obolibrary.org/obo/MONDO_0013052>
|
|
p:direct-normalized/P699
|
<http://purl.obolibrary.org/obo/DOID_DOID:0110386>
|
|
wdt:P11430
|
"DI-02473"
|
|
wdt:P2293
|
KLHL7
|
|
wdt:P279
|
autosomal dominant disease
|
|
retinitis pigmentosa
|
|
wdt:P2888
|
<http://identifiers.org/doid/DOID:0110386>
|
|
<http://purl.obolibrary.org/obo/DOID_0110386>
|
|
wdt:P2892
|
"C2751986"
|
|
wdt:P31
|
type of disease
|
|
rare disease
|
|
wdt:P4229
|
"H35.5"
|
|
wdt:P486
|
"C567854"
|
|
wdt:P492
|
"612943"
|
|
wdt:P5008
|
WikiProject Medicine
|
|
wdt:P5270
|
"MONDO_0013052"
|
|
wdt:P699
|
"DOID:0110386"
|