PMC:7796072 / 482-621
Annnotations
LitCovid-PubTator
{"project":"LitCovid-PubTator","denotations":[{"id":"35","span":{"begin":123,"end":126},"obj":"Gene"},{"id":"45","span":{"begin":71,"end":92},"obj":"Disease"}],"attributes":[{"id":"A35","pred":"tao:has_database_id","subj":"35","obj":"Gene:3046"},{"id":"A45","pred":"tao:has_database_id","subj":"45","obj":"MESH:D013789"}],"namespaces":[{"prefix":"Tax","uri":"https://www.ncbi.nlm.nih.gov/taxonomy/"},{"prefix":"MESH","uri":"https://id.nlm.nih.gov/mesh/"},{"prefix":"Gene","uri":"https://www.ncbi.nlm.nih.gov/gene/"},{"prefix":"CVCL","uri":"https://web.expasy.org/cellosaurus/CVCL_"}],"text":"d between the SE Asian populations, such as the more than 60 different thalassemia syndromes (principally dominated by the HbE trait). In t"}