CORD-19:ee0a7632371a08727d41e55aad7d621daeceef7d / 181327-181351 JSONTXT

{"project":"CORD-19-PD-HP","denotations":[{"id":"T467","span":{"begin":0,"end":24},"obj":"Phenotype"}],"attributes":[{"id":"A467","pred":"hp_id","subj":"T467","obj":"http://purl.obolibrary.org/obo/HP_0002863"}],"text":"myelodysplastic syndrome"}

{"project":"CORD-19-PD-MONDO","denotations":[{"id":"T1158","span":{"begin":0,"end":24},"obj":"Disease"},{"id":"T1148","span":{"begin":0,"end":24},"obj":"Disease"}],"attributes":[{"id":"A1158","pred":"mondo_id","subj":"T1158","obj":"http://purl.obolibrary.org/obo/MONDO_0018881"},{"id":"A1159","pred":"mondo_id","subj":"T1158","obj":"http://purl.obolibrary.org/obo/MONDO_0044873"},{"id":"A79897","pred":"mondo_id","subj":"T1148","obj":"http://purl.obolibrary.org/obo/MONDO_0018881"},{"id":"A44250","pred":"mondo_id","subj":"T1148","obj":"http://purl.obolibrary.org/obo/MONDO_0044873"}],"text":"myelodysplastic syndrome"}