CORD-19:2008f024274c53b0de1276f4047a6a641813fd98 / 186737-186865 JSONTXT

{"project":"CORD-19-Sentences","denotations":[{"id":"T17715","span":{"begin":0,"end":13},"obj":"Sentence"},{"id":"T60854","span":{"begin":14,"end":128},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"CON-CLUSIONS: This case represents a rare manifestation of combined immunodeficiency: the development of a primary CNS lymphoma."}

{"project":"Epistemic_Statements","denotations":[{"id":"T324","span":{"begin":0,"end":128},"obj":"Epistemic_statement"}],"text":"CON-CLUSIONS: This case represents a rare manifestation of combined immunodeficiency: the development of a primary CNS lymphoma."}

{"project":"CORD-19_Custom_license_subset","denotations":[{"id":"T381","span":{"begin":0,"end":13},"obj":"Sentence"},{"id":"T382","span":{"begin":14,"end":128},"obj":"Sentence"}],"text":"CON-CLUSIONS: This case represents a rare manifestation of combined immunodeficiency: the development of a primary CNS lymphoma."}

{"project":"CORD-19-PD-MONDO","denotations":[{"id":"T1696","span":{"begin":59,"end":84},"obj":"Disease"},{"id":"T1697","span":{"begin":68,"end":84},"obj":"Disease"},{"id":"T1698","span":{"begin":107,"end":127},"obj":"Disease"},{"id":"T1699","span":{"begin":119,"end":127},"obj":"Disease"}],"attributes":[{"id":"A1696","pred":"mondo_id","subj":"T1696","obj":"http://purl.obolibrary.org/obo/MONDO_0015131"},{"id":"A1697","pred":"mondo_id","subj":"T1697","obj":"http://purl.obolibrary.org/obo/MONDO_0021094"},{"id":"A1698","pred":"mondo_id","subj":"T1698","obj":"http://purl.obolibrary.org/obo/MONDO_0002571"},{"id":"A1699","pred":"mondo_id","subj":"T1699","obj":"http://purl.obolibrary.org/obo/MONDO_0005062"}],"text":"CON-CLUSIONS: This case represents a rare manifestation of combined immunodeficiency: the development of a primary CNS lymphoma."}

{"project":"CORD-19-PD-HP","denotations":[{"id":"T783","span":{"begin":59,"end":84},"obj":"Phenotype"},{"id":"T784","span":{"begin":107,"end":127},"obj":"Phenotype"}],"attributes":[{"id":"A783","pred":"hp_id","subj":"T783","obj":"http://purl.obolibrary.org/obo/HP_0005387"},{"id":"A784","pred":"hp_id","subj":"T784","obj":"http://purl.obolibrary.org/obo/HP_0030069"}],"text":"CON-CLUSIONS: This case represents a rare manifestation of combined immunodeficiency: the development of a primary CNS lymphoma."}

{"project":"CORD-19-PD-UBERON","denotations":[{"id":"T347","span":{"begin":115,"end":118},"obj":"Body_part"}],"attributes":[{"id":"A347","pred":"uberon_id","subj":"T347","obj":"http://purl.obolibrary.org/obo/UBERON_0001017"}],"text":"CON-CLUSIONS: This case represents a rare manifestation of combined immunodeficiency: the development of a primary CNS lymphoma."}