pldy6taj | Knowledge4COVID-19

Property	Value
is ?:annotates of	<https://research.tib.eu/covid-19/entity/pldy6taj_hasAnnotation_C1822777> <https://research.tib.eu/covid-19/entity/pldy6taj_hasAnnotation_C2985439>
?:creator	<https://research.tib.eu/covid-19/entity/Fang%2C_Hongjun%3B_Zhang%2C_Xi%3B_Xiao%2C_Bo%3B_Zhang%2C_Lily%3B_Long%2C_Hongyu>
?:doi	<https://research.tib.eu/covid-19/entity/10.1007/s10072-020-04559-3>
?:doi	10.1007/s10072-020-04559-3
?:journal	Neurological_sciences_:_official_journal_of_the_Italian_Neurological_Society_and_of_the_Italian_Society_of_Clinical_Neurophysiology
?:license	unk
?:pmid	<https://research.tib.eu/covid-19/entity/32648047>
?:pmid	32648047
?:publication_isRelatedTo_Disease	<https://research.tib.eu/covid-19/entity/COVID-19>
?:source	Medline
?:title	A de novo mutation in SMC1A gene identified in a Chinese infant with nonclassical Cornelia de Lange syndrome and drug-resistant epilepsy.
?:type	<https://research.tib.eu/covid-19/vocab/Publication>
?:year	2020-07-10

Metadata

Anon_0

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Anon_0

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