PubMed:8106452 / 215-486 JSONTXT

{"project":"sentences","denotations":[{"id":"TextSentencer_T2","span":{"begin":0,"end":271},"obj":"Sentence"},{"id":"T2","span":{"begin":0,"end":271},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"Deficiency of the lysosomal enzyme beta-hexosaminidase B (beta-Hex B) (a homodimer, beta beta), caused by a defect in the HEX B gene encoding the beta-chain, is usually accompanied by an absence of beta-Hex A (a heterodimer, alpha beta), thereby causing Sandhoff disease."}

{"project":"DisGeNET5_gene_disease","denotations":[{"id":"8106452-1#35#54#gene10724","span":{"begin":35,"end":54},"obj":"gene10724"},{"id":"8106452-1#203#206#gene10724","span":{"begin":203,"end":206},"obj":"gene10724"},{"id":"8106452-1#254#270#diseaseC0036161","span":{"begin":254,"end":270},"obj":"diseaseC0036161"}],"relations":[{"id":"35#54#gene10724254#270#diseaseC0036161","pred":"associated_with","subj":"8106452-1#35#54#gene10724","obj":"8106452-1#254#270#diseaseC0036161"},{"id":"203#206#gene10724254#270#diseaseC0036161","pred":"associated_with","subj":"8106452-1#203#206#gene10724","obj":"8106452-1#254#270#diseaseC0036161"}],"text":"Deficiency of the lysosomal enzyme beta-hexosaminidase B (beta-Hex B) (a homodimer, beta beta), caused by a defect in the HEX B gene encoding the beta-chain, is usually accompanied by an absence of beta-Hex A (a heterodimer, alpha beta), thereby causing Sandhoff disease."}

{"project":"PubCasesORDO","denotations":[{"id":"AB1","span":{"begin":254,"end":270},"obj":"ORDO:796"}],"namespaces":[{"prefix":"ORDO","uri":"http://www.orpha.net/ORDO/Orphanet_"}],"text":"Deficiency of the lysosomal enzyme beta-hexosaminidase B (beta-Hex B) (a homodimer, beta beta), caused by a defect in the HEX B gene encoding the beta-chain, is usually accompanied by an absence of beta-Hex A (a heterodimer, alpha beta), thereby causing Sandhoff disease."}

{"project":"mondo_disease","denotations":[{"id":"T2","span":{"begin":254,"end":270},"obj":"Disease"}],"attributes":[{"id":"A2","pred":"mondo_id","subj":"T2","obj":"http://purl.obolibrary.org/obo/MONDO_0010006"}],"text":"Deficiency of the lysosomal enzyme beta-hexosaminidase B (beta-Hex B) (a homodimer, beta beta), caused by a defect in the HEX B gene encoding the beta-chain, is usually accompanied by an absence of beta-Hex A (a heterodimer, alpha beta), thereby causing Sandhoff disease."}