CORD-19:ee0a7632371a08727d41e55aad7d621daeceef7d / 175303-175542
Annnotations
CORD-19-Sentences
{"project":"CORD-19-Sentences","denotations":[{"id":"T42156","span":{"begin":0,"end":239},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"First recognized as a distinct entity in 1938, Diamond Blackfan anemia (DBA) is a genetically and clinically heterogeneous disorder characterized by pure red blood cell aplasia, variable congenital anomalies and a predisposition to cancer."}
CORD-19_Custom_license_subset
{"project":"CORD-19_Custom_license_subset","denotations":[{"id":"T428","span":{"begin":0,"end":239},"obj":"Sentence"}],"text":"First recognized as a distinct entity in 1938, Diamond Blackfan anemia (DBA) is a genetically and clinically heterogeneous disorder characterized by pure red blood cell aplasia, variable congenital anomalies and a predisposition to cancer."}
CORD-19-PD-HP
{"project":"CORD-19-PD-HP","denotations":[{"id":"T442","span":{"begin":64,"end":70},"obj":"Phenotype"},{"id":"T443","span":{"begin":232,"end":238},"obj":"Phenotype"}],"attributes":[{"id":"A442","pred":"hp_id","subj":"T442","obj":"http://purl.obolibrary.org/obo/HP_0001903"},{"id":"A443","pred":"hp_id","subj":"T443","obj":"http://purl.obolibrary.org/obo/HP_0002664"}],"text":"First recognized as a distinct entity in 1938, Diamond Blackfan anemia (DBA) is a genetically and clinically heterogeneous disorder characterized by pure red blood cell aplasia, variable congenital anomalies and a predisposition to cancer."}
CORD-19-PD-UBERON
{"project":"CORD-19-PD-UBERON","denotations":[{"id":"T138","span":{"begin":158,"end":163},"obj":"Body_part"}],"attributes":[{"id":"A138","pred":"uberon_id","subj":"T138","obj":"http://purl.obolibrary.org/obo/UBERON_0000178"}],"text":"First recognized as a distinct entity in 1938, Diamond Blackfan anemia (DBA) is a genetically and clinically heterogeneous disorder characterized by pure red blood cell aplasia, variable congenital anomalies and a predisposition to cancer."}
CORD-19-PD-MONDO
{"project":"CORD-19-PD-MONDO","denotations":[{"id":"T1117","span":{"begin":47,"end":70},"obj":"Disease"},{"id":"T1118","span":{"begin":64,"end":70},"obj":"Disease"},{"id":"T1119","span":{"begin":72,"end":75},"obj":"Disease"},{"id":"T1120","span":{"begin":187,"end":207},"obj":"Disease"},{"id":"T1121","span":{"begin":232,"end":238},"obj":"Disease"},{"id":"T81843","span":{"begin":47,"end":70},"obj":"Disease"},{"id":"T1108","span":{"begin":64,"end":70},"obj":"Disease"},{"id":"T25380","span":{"begin":72,"end":75},"obj":"Disease"},{"id":"T63239","span":{"begin":187,"end":207},"obj":"Disease"},{"id":"T1111","span":{"begin":232,"end":238},"obj":"Disease"}],"attributes":[{"id":"A1117","pred":"mondo_id","subj":"T1117","obj":"http://purl.obolibrary.org/obo/MONDO_0015253"},{"id":"A1118","pred":"mondo_id","subj":"T1118","obj":"http://purl.obolibrary.org/obo/MONDO_0002280"},{"id":"A1119","pred":"mondo_id","subj":"T1119","obj":"http://purl.obolibrary.org/obo/MONDO_0015253"},{"id":"A1120","pred":"mondo_id","subj":"T1120","obj":"http://purl.obolibrary.org/obo/MONDO_0000839"},{"id":"A1121","pred":"mondo_id","subj":"T1121","obj":"http://purl.obolibrary.org/obo/MONDO_0004992"},{"id":"A68916","pred":"mondo_id","subj":"T81843","obj":"http://purl.obolibrary.org/obo/MONDO_0015253"},{"id":"A46962","pred":"mondo_id","subj":"T1108","obj":"http://purl.obolibrary.org/obo/MONDO_0002280"},{"id":"A70316","pred":"mondo_id","subj":"T25380","obj":"http://purl.obolibrary.org/obo/MONDO_0015253"},{"id":"A26994","pred":"mondo_id","subj":"T63239","obj":"http://purl.obolibrary.org/obo/MONDO_0000839"}],"text":"First recognized as a distinct entity in 1938, Diamond Blackfan anemia (DBA) is a genetically and clinically heterogeneous disorder characterized by pure red blood cell aplasia, variable congenital anomalies and a predisposition to cancer."}