C3810326 | Knowledge4COVID-19

Property	Value
?:annLabel	Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to run and cysteine rich domain containing beclin 1 interacting protein deficiency (disorder)
?:annotationFrequency	2 ()
is ?:hasCUIAnnotation of	<https://research.tib.eu/covid-19/entity/Autosomal%20recessive%20cerebellar%20ataxia%2C%20epilepsy%2C%20intellectual%20disability%20syndrome%20due%20to%20run%20and%20cysteine%20rich%20domain%20containing%20beclin%201%20interacting%20protein%20deficiency%20%28disorder%29> <https://research.tib.eu/covid-19/entity/C3810326_SCTSPA> <https://research.tib.eu/covid-19/entity/C3810326_SNOMEDCT_US> <https://research.tib.eu/covid-19/entity/C3810326_T047>
?:sameAs	<http://dbpedia.org/resource/Autosomal_recessive_cerebellar_ataxia> <http://www.wikidata.org/entity/Q21124566>
?:type	<https://research.tib.eu/covid-19/vocab/Annotation>

Metadata

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