CORD-19:120bd6eed7e254029455aec25478a4860a46764e / 190891-191164 JSONTXT

{"project":"CORD-19-SciBite-sentences","denotations":[{"id":"T3011","span":{"begin":0,"end":273},"obj":"https://id.nlm.nih.gov/mesh/D006008"},{"id":"T3012","span":{"begin":0,"end":273},"obj":"https://id.nlm.nih.gov/mesh/D009083"},{"id":"T3013","span":{"begin":0,"end":273},"obj":"https://id.nlm.nih.gov/mesh/D016464"}],"attributes":[{"id":"A3011","pred":"class","subj":"T3011","obj":"INDICATION"},{"id":"A3012","pred":"class","subj":"T3012","obj":"INDICATION"},{"id":"A3013","pred":"class","subj":"T3013","obj":"INDICATION"}],"text":"Examples of autosomal recessive disorders in animals include lysosomal storage diseases (see , glycogen storage diseases (see Fig. 14-63) and mucopolysaccharidoses, and aminoacidopathies that affect organs such as the brain, spinal cord, skeletal muscle, liver, and kidney."}

{"project":"CORD-19_Custom_license_subset","denotations":[{"id":"T302","span":{"begin":0,"end":273},"obj":"Sentence"}],"text":"Examples of autosomal recessive disorders in animals include lysosomal storage diseases (see , glycogen storage diseases (see Fig. 14-63) and mucopolysaccharidoses, and aminoacidopathies that affect organs such as the brain, spinal cord, skeletal muscle, liver, and kidney."}

{"project":"CORD-19-Sentences","denotations":[{"id":"TextSentencer_T1277","span":{"begin":0,"end":273},"obj":"Sentence"},{"id":"TextSentencer_T1277","span":{"begin":0,"end":273},"obj":"Sentence"},{"id":"T26016","span":{"begin":0,"end":273},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"Examples of autosomal recessive disorders in animals include lysosomal storage diseases (see , glycogen storage diseases (see Fig. 14-63) and mucopolysaccharidoses, and aminoacidopathies that affect organs such as the brain, spinal cord, skeletal muscle, liver, and kidney."}

{"project":"CORD-19-PD-MONDO","denotations":[{"id":"T615","span":{"begin":61,"end":87},"obj":"Disease"},{"id":"T616","span":{"begin":95,"end":120},"obj":"Disease"},{"id":"T617","span":{"begin":142,"end":163},"obj":"Disease"}],"attributes":[{"id":"A615","pred":"mondo_id","subj":"T615","obj":"http://purl.obolibrary.org/obo/MONDO_0002561"},{"id":"A616","pred":"mondo_id","subj":"T616","obj":"http://purl.obolibrary.org/obo/MONDO_0002412"},{"id":"A617","pred":"mondo_id","subj":"T617","obj":"http://purl.obolibrary.org/obo/MONDO_0019249"}],"text":"Examples of autosomal recessive disorders in animals include lysosomal storage diseases (see , glycogen storage diseases (see Fig. 14-63) and mucopolysaccharidoses, and aminoacidopathies that affect organs such as the brain, spinal cord, skeletal muscle, liver, and kidney."}

{"project":"CORD-19-PD-UBERON","denotations":[{"id":"T653","span":{"begin":199,"end":205},"obj":"Body_part"},{"id":"T654","span":{"begin":218,"end":223},"obj":"Body_part"},{"id":"T655","span":{"begin":225,"end":236},"obj":"Body_part"},{"id":"T656","span":{"begin":255,"end":260},"obj":"Body_part"},{"id":"T657","span":{"begin":266,"end":272},"obj":"Body_part"}],"attributes":[{"id":"A653","pred":"uberon_id","subj":"T653","obj":"http://purl.obolibrary.org/obo/UBERON_0000062"},{"id":"A654","pred":"uberon_id","subj":"T654","obj":"http://purl.obolibrary.org/obo/UBERON_0000955"},{"id":"A655","pred":"uberon_id","subj":"T655","obj":"http://purl.obolibrary.org/obo/UBERON_0002240"},{"id":"A656","pred":"uberon_id","subj":"T656","obj":"http://purl.obolibrary.org/obo/UBERON_0002107"},{"id":"A657","pred":"uberon_id","subj":"T657","obj":"http://purl.obolibrary.org/obo/UBERON_0002113"}],"text":"Examples of autosomal recessive disorders in animals include lysosomal storage diseases (see , glycogen storage diseases (see Fig. 14-63) and mucopolysaccharidoses, and aminoacidopathies that affect organs such as the brain, spinal cord, skeletal muscle, liver, and kidney."}