|
rdfs:label
|
"Distrofia da retina, genética"@pt
"Distrofia da retina, genética"@pt-br
"Distrofias de la retina"@es
"Netzhautdystrophie"@de
"distrofija fundusa"@sl
"distròfia de fons"@ca
"dystrophie de la rétine"@fr
"fundus dystrophy"@en
|
|
skos:altLabel
|
"Retinal Dystrophy"@en
"distrofija očesnega ozadja"@sl
"dystrophie du fond d'oeil"@fr
"fundus dystrophies"@en
"retinal dystrophies"@en
|
|
schema:description
|
"Augenkrankheit"@de
"human disease"@en
"malaltia humana"@ca
"serie de enfermedades hereditarias de la retina"@es
"хвороба людини"@uk
"մարդու հիվանդություն"@hy
"مرض يصيب الإنسان"@ar
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|
schema:dateModified
|
"2026-10-24T00:32:42+00:00"^^xsd:dateTime
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schema:version
|
2560166729
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|
wikibase:identifiers
|
10
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|
8
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wikibase:sitelinks
|
2
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wikibase:statements
|
102
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p:P2888
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wd:statement/Q5811451-016AC742-5872-469D-9526-D9843176A64C
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wd:statement/Q5811451-254336FC-E3BC-408A-A6D4-EB5E00A8A1BC
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wd:statement/Q5811451-634AD766-E9BF-404E-BB4E-BA58BAF25279
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wd:statement/Q5811451-9ACDEADC-1700-438D-BFFA-0B67A9CDFBFF
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p:P2892
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wd:statement/Q5811451-66729879-26D6-4FA5-822C-87FCEA72B062
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p:P31
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wd:statement/Q5811451-3FD1387A-014C-460D-AA90-D882CCC28240
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|
p:P3841
|
wd:statement/Q5811451-2DB7F397-FB97-4B39-94CF-AC32806DFA56
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|
p:P486
|
wd:statement/Q5811451-77FBB284-1DE2-425D-84CF-FA9ECE52096C
|
|
p:P5008
|
wd:statement/Q5811451-8D46F198-AFBC-4C38-8186-8C79838A278D
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|
p:P5270
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wd:statement/Q5811451-A8A184AB-A85A-4D98-867B-2D6B8FDF2FD7
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|
p:P557
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wd:statement/Q5811451-57CA3501-22C9-46D8-A7EA-B7525FAD484C
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p:P672
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wd:statement/Q5811451-B16C470A-8838-4BEA-81C2-B7985E46AB9E
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p:P699
|
wd:statement/Q5811451-E5B33463-12A3-4A67-AE1D-710940F2A224
|
|
p:direct-normalized/P486
|
<http://id.nlm.nih.gov/mesh/D058499>
|
|
p:direct-normalized/P5270
|
<http://purl.obolibrary.org/obo/MONDO_0019118>
|
|
p:direct-normalized/P672
|
<http://id.nlm.nih.gov/mesh/C11.768.585.658>
|
|
p:direct-normalized/P699
|
<http://purl.obolibrary.org/obo/DOID_DOID:8501>
|
|
wdt:P14914
|
"D71862"
|
|
wdt:P1550
|
"71862"
|
|
wdt:P1692
|
"362.72"
|
|
"362.75"
|
|
wdt:P1748
|
"C35625"
|
|
wdt:P1995
|
ophthalmology
|
|
wdt:P2293
|
RHO
|
|
PROM1
|
|
RBP4
|
|
PAX6
|
|
AHR
|
|
LRAT
|
|
ABCA4
|
|
ACO2
|
|
BBS1
|
|
BBS2
|
|
CACNA1F
|
|
CDH3
|
|
CNGA1
|
|
CNGA3
|
|
CRX
|
|
FBN2
|
|
GNAT2
|
|
IDH3A
|
|
MAK
|
|
OAT
|
|
OTX2
|
|
PDE6A
|
|
PDE6G
|
|
OPN1LW
|
|
RDH5
|
|
PRPH2
|
|
GRK1
|
|
RLBP1
|
|
ROM1
|
|
RP1
|
|
RPGR
|
|
RPE65
|
|
RS1
|
|
SAG
|
|
CLEC3B
|
|
USH2A
|
|
BEST1
|
|
ADAM9
|
|
RAB28
|
|
IFT140
|
|
TOPORS
|
|
TUBB4B
|
|
MERTK
|
|
FBLN5
|
|
TREX1
|
|
SNRNP200
|
|
ARHGEF18
|
|
ARL2BP
|
|
AIPL1
|
|
IFT172
|
|
TINF2
|
|
IMPG2
|
|
RCBTB1
|
|
SPATA7
|
|
KIZ
|
|
RPGRIP1
|
|
SLC7A14
|
|
CEP290
|
|
HKDC1
|
|
TLCD3B
|
|
ARL6
|
|
FAM161A
|
|
RAX2
|
|
TUBGCP6
|
|
RP1L1
|
|
TTC8
|
|
CLDN19
|
|
CFAP418
|
|
LCA5
|
|
MFSD8
|
|
CYP4V2
|
|
LRIT3
|
|
CERKL
|
|
PCARE
|
|
GPR179
|
|
KIF11
|
|
IMPDH1
|
|
PRCD
|
|
PRPF3
|
|
PRPF31
|
|
wdt:P279
|
retinal degeneration
|
|
genetic vitreous-retinal disease
|
|
wdt:P2888
|
<http://identifiers.org/doid/DOID:8501>
|
|
<http://purl.obolibrary.org/obo/DOID_8501>
|
|
<http://purl.obolibrary.org/obo/HP_0000556>
|
|
<http://www.orpha.net/ORDO/Orphanet_71862>
|
|
wdt:P2892
|
"C0854723"
|
|
wdt:P31
|
type of disease
|
|
wdt:P3841
|
"HP:0000556"
|
|
wdt:P486
|
"D058499"
|
|
wdt:P5008
|
WikiProject Medicine
|
|
wdt:P5270
|
"MONDO_0019118"
|
|
wdt:P557
|
"9580"
|
|
wdt:P672
|
"C11.768.585.658"
|
|
wdt:P699
|
"DOID:8501"
|