PubMed:8106452 / 215-486
Annnotations
sentences
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| TextSentencer_T2 | 0-271 | Sentence | denotes | 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. |
| T2 | 0-271 | Sentence | denotes | 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. |
DisGeNET5_gene_disease
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| 8106452-1#35#54#gene10724 | 35-54 | gene10724 | denotes | beta-hexosaminidase |
| 8106452-1#203#206#gene10724 | 203-206 | gene10724 | denotes | Hex |
| 8106452-1#254#270#diseaseC0036161 | 254-270 | diseaseC0036161 | denotes | Sandhoff disease |
| 35#54#gene10724254#270#diseaseC0036161 | 8106452-1#35#54#gene10724 | 8106452-1#254#270#diseaseC0036161 | associated_with | beta-hexosaminidase,Sandhoff disease |
| 203#206#gene10724254#270#diseaseC0036161 | 8106452-1#203#206#gene10724 | 8106452-1#254#270#diseaseC0036161 | associated_with | Hex,Sandhoff disease |
PubCasesORDO
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| AB1 | 254-270 | ORDO:796 | denotes | Sandhoff disease |
mondo_disease
| Id | Subject | Object | Predicate | Lexical cue | mondo_id |
|---|---|---|---|---|---|
| T2 | 254-270 | Disease | denotes | Sandhoff disease | http://purl.obolibrary.org/obo/MONDO_0010006 |