C5192431 | Knowledge4COVID-19

Property	Value
?:annLabel	Developmental delay, facial dysmorphism syndrome due to med13l deficiency
?:annotationFrequency	1 ()
is ?:hasCUIAnnotation of	<https://research.tib.eu/covid-19/entity/C5192431_SCTSPA> <https://research.tib.eu/covid-19/entity/C5192431_SNOMEDCT_US> <https://research.tib.eu/covid-19/entity/C5192431_T047> <https://research.tib.eu/covid-19/entity/Developmental%20delay%2C%20facial%20dysmorphism%20syndrome%20due%20to%20med13l%20deficiency>
?:sameAs	<http://dbpedia.org/resource/Specific_developmental_disorder> <http://www.wikidata.org/entity/Q55783259>
?:type	<https://research.tib.eu/covid-19/vocab/Annotation>

Metadata

Anon_0

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Anon_0

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Anon_1 (more)

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