progressive epilepsy and/or ataxia with myoclonus as a major feature
human disease
| rdfs:label | "progressive epilepsy and/or ataxia with myoclonus as a major feature"@en |
| schema:description |
"human disease"@en
|
|
schema:date |
"2024-02-26T18:53:04+00:00"^^xsd:dateTime |
| schema:version | 2088042202 |
| wikibase:identifiers | 2 |
| wikibase:sitelinks | 0 |
| wikibase:statements | 6 |
| p:P1550 | wd:statement/Q55787255-6017C610-80E1-4CC5-8585-7BDC14F135B7 |
| p:P279 | wd:statement/Q55787255-809742FE-B944-49D2-997E-874E4D651580 |
| wd:statement/Q55787255-F61E4C1E-96C1-47FA-AD08-DC5410EBFEC2 | |
| p:P2888 | wd:statement/Q55787255-2D0480F0-41E9-4A42-9241-C931A16DBA51 |
| p:P31 | wd:statement/Q55787255-52146BD5-F9C2-498E-8C9F-00175C71B56C |
| p:P5270 | wd:statement/Q55787255-E880EC71-EA6B-41C7-A8C4-28E30C324679 |
|
p:direct- |
<http:/ |
| wdt:P1550 | "306762" |
| wdt:P279 | rare genetic epilepsy |
| epilepsy and/or ataxia with myoclonus as major feature | |
| wdt:P2888 |
<http:/ |
| wdt:P31 | type of disease |
| wdt:P5270 | "MONDO_0017655" |
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