SHMARQL

neuronal ceroid lipofuscinosis

<http://www.wikidata.org/entity/Q4358039>

human disease
rdfs:label
"neuronal ceroid lipofuscinosis"@en
skos:altLabel
"NCL"@en
"Neuronal Ceroid-Lipofuscinoses"@en
"hereditary ceroid lipofuscinosis"@en
"neuronal ceroid lipofuscinosis (disorder)"@en
schema:description
"human disease"@en
schema:dateModified "2026-10-23T23:39:17+00:00"^^xsd:dateTime
schema:version 2560157011
wikibase:identifiers 26
28
wikibase:sitelinks 11
wikibase:statements 53
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wd:statement/Q4358039-619F9637-73CC-4983-BEC5-FFADF598286A
wd:statement/Q4358039-99861212-4E30-4EF2-B49F-C97285C4E9DB
wd:statement/Q4358039-A8FCCF60-1B8B-464A-9716-D017C25496CB
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p:P665 wd:statement/Q4358039-461895BE-F252-4300-BC09-1FD6C7944C7D
p:P672 wd:statement/Q4358039-1C63BE13-8FCF-4FEE-A53F-726B8A1B2BA1
wd:statement/Q4358039-78C115B4-8C3D-462A-A207-435B53A5C411
wd:statement/Q4358039-7CDD978D-4949-42EF-BA7A-EAE2A46583CB
wd:statement/Q4358039-9C9B8885-2BB1-4498-952A-908C52F0998A
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p:P7807 wd:statement/Q4358039-0E6C3FE4-B61E-47BB-8582-35983733DFCD
p:P8189 wd:statement/Q4358039-F0F34242-820A-48F5-AD7B-35F59A990B96
p:direct-normalized/P2347 <http://www.yso.fi/onto/yso/p582>
p:direct-normalized/P244 <http://id.loc.gov/authorities/names/sh85091152>
p:direct-normalized/P2581 <http://babelnet.org/rdf/s01481411n>
p:direct-normalized/P486 <http://id.nlm.nih.gov/mesh/D009472>
p:direct-normalized/P5270 <http://purl.obolibrary.org/obo/MONDO_0016295>
p:direct-normalized/P6366 <https://makg.org/entity/2778650512>
p:direct-normalized/P665 <http://www.kegg.jp/entry/H00149>
p:direct-normalized/P672 <http://id.nlm.nih.gov/mesh/C10.574.500.550>
<http://id.nlm.nih.gov/mesh/C16.320.400.600>
<http://id.nlm.nih.gov/mesh/C16.320.565.398.641.509>
<http://id.nlm.nih.gov/mesh/C18.452.584.563.641.509>
<http://id.nlm.nih.gov/mesh/C18.452.648.398.641.509>
p:direct-normalized/P699 <http://purl.obolibrary.org/obo/DOID_DOID:14503>
wdt:P10283 "C2778650512"
wdt:P11143 "Neuronal ceroid lipofuscinosis"
wdt:P1343 The Unified Medical Dictionary (Librairie du Liban, 2009)
wdt:P13591 "concept/f71b5639-3c00-431d-86e1-bd59f3d2128a"
wdt:P14914 "D00216"
wdt:P1550 "216"
"79262"
wdt:P1748 "C61257"
wdt:P1995 endocrinology
wdt:P2293 CLN3
CLN5
CLN8
TPP1
GRN
PPT1
CTSF
ATP13A2
CLN6
DNAJC5
KCTD7
MFSD8
CTSD
wdt:P2347 "582"
wdt:P244 "sh85091152"
wdt:P2581 "01481411n"
wdt:P279 eye degenerative disease
nervous system heredodegenerative disease
lipid storage disease
wdt:P2841 any age
wdt:P2888 <http://identifiers.org/doid/DOID:14503>
<http://purl.obolibrary.org/obo/DOID_14503>
<http://www.orpha.net/ORDO/Orphanet_216>
<http://www.orpha.net/ORDO/Orphanet_79262>
wdt:P2892 "C0027877"
wdt:P31 type of disease
wdt:P4229 "E75.4"
wdt:P4317 "10739"
wdt:P486 "D009472"
wdt:P5008 WikiProject Medicine
wdt:P5270 "MONDO_0016295"
wdt:P604 "001613"
wdt:P6366 "2778650512"
wdt:P665 "H00149"
wdt:P672 "C10.574.500.550"
"C16.320.400.600"
"C16.320.565.398.641.509"
"C18.452.584.563.641.509"
"C18.452.648.398.641.509"
wdt:P673 "1178391"
wdt:P699 "DOID:14503"
wdt:P7329 "5C56.1"
wdt:P7807 "1568332253"
wdt:P8189 "987012431017605171"
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data from SPARQL profile: Wikidata