C3809971 | Knowledge4COVID-19

Property	Value
?:annLabel	Congenital microcephaly, severe encephalopathy, progressive cerebral atrophy syndrome (disorder)
?:annotationFrequency	2 ()
is ?:hasCUIAnnotation of	<https://research.tib.eu/covid-19/entity/C3809971_NCI> <https://research.tib.eu/covid-19/entity/C3809971_SCTSPA> <https://research.tib.eu/covid-19/entity/C3809971_SNOMEDCT_US> <https://research.tib.eu/covid-19/entity/C3809971_T047> <https://research.tib.eu/covid-19/entity/Congenital%20microcephaly%2C%20severe%20encephalopathy%2C%20progressive%20cerebral%20atrophy%20syndrome%20%28disorder%29>
?:sameAs	<http://dbpedia.org/resource/Congenital_disorder> <http://www.wikidata.org/entity/Q18966152>
?:type	<https://research.tib.eu/covid-19/vocab/Annotation>

Metadata

Anon_0

<http://www.w3.org/1999/02/22-rdf-syntax-ns#type>

<http://purl.org/net/provenance/ns#DataItem>

<http://www.w3.org/1999/02/22-rdf-syntax-ns#type>

<http://www.w3.org/2004/03/trix/rdfg-1/Graph>

<http://xmlns.com/foaf/0.1/primaryTopic>

<https://research.tib.eu/covid-19/entity/C3809971>

<http://xmlns.com/foaf/0.1/topic>

Anon_0

<http://www.ontologydesignpatterns.org/cp/owl/informationrealization.owl#realizes>

<https://research.tib.eu/covid-19/data/entity/C3809971>

<http://purl.org/net/provenance/ns#createdBy>

Anon_1 (more)

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