CORD-19:775b90287b44353bee979abb0970a4666022f86d / 606854-606878 JSONTXT

{"project":"CORD-19-PD-MONDO","denotations":[{"id":"T4663","span":{"begin":0,"end":24},"obj":"Disease"},{"id":"T86035","span":{"begin":0,"end":24},"obj":"Disease"}],"attributes":[{"id":"A4663","pred":"mondo_id","subj":"T4663","obj":"http://purl.obolibrary.org/obo/MONDO_0018881"},{"id":"A4664","pred":"mondo_id","subj":"T4663","obj":"http://purl.obolibrary.org/obo/MONDO_0044873"},{"id":"A58234","pred":"mondo_id","subj":"T86035","obj":"http://purl.obolibrary.org/obo/MONDO_0018881"},{"id":"A97102","pred":"mondo_id","subj":"T86035","obj":"http://purl.obolibrary.org/obo/MONDO_0044873"}],"text":"myelodysplastic syndrome"}

{"project":"CORD-19-PD-HP","denotations":[{"id":"T3325","span":{"begin":0,"end":24},"obj":"Phenotype"}],"attributes":[{"id":"A3325","pred":"hp_id","subj":"T3325","obj":"http://purl.obolibrary.org/obo/HP_0002863"}],"text":"myelodysplastic syndrome"}