CORD-19:3f9572ae671d876279b4d2cd6b6544b24fb3e52d / 7908-8204
Annnotations
{"target":"https://pubannotation.org/docs/sourcedb/CORD-19/sourceid/3f9572ae671d876279b4d2cd6b6544b24fb3e52d","sourcedb":"CORD-19","sourceid":"3f9572ae671d876279b4d2cd6b6544b24fb3e52d","text":"48 Five different mutations in the coding region of the stefin B gene were found causing protein truncation (R68X), frameshift (K73fsX2) and missense mutations (G4R, Q71P and G50E). [49] [50] [51] [52] [53] Stefin B normally localizes in the nucleus, cytoplasm and also associates with lysosomes.","tracks":[{"project":"CORD-19-Sentences","denotations":[{"id":"TextSentencer_T46","span":{"begin":0,"end":296},"obj":"Sentence"},{"id":"TextSentencer_T46","span":{"begin":0,"end":296},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"attributes":[{"subj":"TextSentencer_T46","pred":"source","obj":"CORD-19-Sentences"},{"subj":"TextSentencer_T46","pred":"source","obj":"CORD-19-Sentences"}]}],"config":{"attribute types":[{"pred":"source","value type":"selection","values":[{"id":"CORD-19-Sentences","color":"#93ecd9","default":true}]}]}}