PMC:7274950 / 9819-9983
Annnotations
LitCovid-PMC-OGER-BB
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T130 | 77-86 | GO:0005764 | denotes | lysosomal |
| T131 | 136-157 | CHEBI:37395;CHEBI:37395 | denotes | mucopolysaccharidoses |
| T23169 | 77-86 | GO:0005764 | denotes | lysosomal |
| T56588 | 136-157 | CHEBI:37395;CHEBI:37395 | denotes | mucopolysaccharidoses |
LitCovid-PubTator
| Id | Subject | Object | Predicate | Lexical cue | tao:has_database_id |
|---|---|---|---|---|---|
| 265 | 87-131 | Disease | denotes | storage diseases like Gaucher disease type I | MESH:D005776 |
| 266 | 159-162 | Disease | denotes | MPS | MESH:D009084 |
LitCovid-PD-FMA-UBERON
| Id | Subject | Object | Predicate | Lexical cue | fma_id |
|---|---|---|---|---|---|
| T52 | 77-86 | Body_part | denotes | lysosomal | http://purl.org/sig/ont/fma/fma63836 |
LitCovid-PD-MONDO
| Id | Subject | Object | Predicate | Lexical cue | mondo_id |
|---|---|---|---|---|---|
| T55 | 77-103 | Disease | denotes | lysosomal storage diseases | http://purl.obolibrary.org/obo/MONDO_0002561 |
| T56 | 109-131 | Disease | denotes | Gaucher disease type I | http://purl.obolibrary.org/obo/MONDO_0009265 |
| T57 | 109-124 | Disease | denotes | Gaucher disease | http://purl.obolibrary.org/obo/MONDO_0018150 |
| T58 | 136-157 | Disease | denotes | mucopolysaccharidoses | http://purl.obolibrary.org/obo/MONDO_0019249 |
| T59 | 159-162 | Disease | denotes | MPS | http://purl.obolibrary.org/obo/MONDO_0019249 |
LitCovid-PD-CLO
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T114 | 77-86 | http://purl.obolibrary.org/obo/GO_0005764 | denotes | lysosomal |
LitCovid-PD-GO-BP
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T6 | 87-94 | http://purl.obolibrary.org/obo/GO_0051235 | denotes | storage |
LitCovid-sentences
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T73 | 0-164 | Sentence | denotes | Effects of temporary ERT interruption were described in more detail in other lysosomal storage diseases like Gaucher disease type I and mucopolysaccharidoses (MPS). |