PubMed:25138275 / 847-1114
Annnotations
ggdb-test
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T7 | 67-72 | https://acgg.asia/db/ggdb/info/gg171 | denotes | LARGE |
| T8 | 256-261 | https://acgg.asia/db/ggdb/info/gg171 | denotes | LARGE |
GGDB-2020
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T7 | 67-72 | https://acgg.asia/db/ggdb/info/gg171 | denotes | LARGE |
| T8 | 256-261 | https://acgg.asia/db/ggdb/info/gg171 | denotes | LARGE |
sentences
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T6 | 0-267 | Sentence | denotes | We show that normal mouse and human cultured cells have endogenous LARGE GlcA-T, and that this activity is absent in cells from the Large(myd) (Large-deficient) mouse model of muscular dystrophy, as well as in cells from CMD patients with mutations in the LARGE gene. |
PubmedHPO
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T4 | 176-194 | HP_0003560 | denotes | muscular dystrophy |
glycogenes
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| PD-GlycoGenes20190927-B_T9 | 67-72 | https://acgg.asia/db/ggdb/info/gg171 | denotes | LARGE |
| PD-GlycoGenes20190927-B_T10 | 73-79 | https://acgg.asia/db/ggdb/info/gg156 | denotes | GlcA-T |
| PD-GlycoGenes20190927-B_T11 | 132-137 | https://acgg.asia/db/ggdb/info/gg171 | denotes | Large |
| PD-GlycoGenes20190927-B_T12 | 144-149 | https://acgg.asia/db/ggdb/info/gg171 | denotes | Large |
| PD-GlycoGenes20190927-B_T13 | 256-261 | https://acgg.asia/db/ggdb/info/gg171 | denotes | LARGE |
PubCasesHPO
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| AB2 | 178-196 | HP:0003560 | denotes | scular dystrophy, |
mondo_disease
| Id | Subject | Object | Predicate | Lexical cue | mondo_id |
|---|---|---|---|---|---|
| T6 | 176-194 | Disease | denotes | muscular dystrophy | http://purl.obolibrary.org/obo/MONDO_0020121 |
| T7 | 221-224 | Disease | denotes | CMD | http://purl.obolibrary.org/obo/MONDO_0007251|http://purl.obolibrary.org/obo/MONDO_0007397|http://purl.obolibrary.org/obo/MONDO_0019950|http://purl.obolibrary.org/obo/MONDO_0044875 |
HP-phenotype
| Id | Subject | Object | Predicate | Lexical cue | hp_id |
|---|---|---|---|---|---|
| T3 | 176-194 | Phenotype | denotes | muscular dystrophy | HP:0003560 |
| T4 | 221-224 | Phenotype | denotes | CMD | HP:0003560 |
NCBITAXON
| Id | Subject | Object | Predicate | Lexical cue | db_id |
|---|---|---|---|---|---|
| T2 | 20-25 | OrganismTaxon | denotes | mouse | 10088|10090 |
| T4 | 30-35 | OrganismTaxon | denotes | human | 9606 |
| T5 | 161-166 | OrganismTaxon | denotes | mouse | 10088|10090 |
CL-cell
| Id | Subject | Object | Predicate | Lexical cue | cl_id |
|---|---|---|---|---|---|
| T1 | 36-50 | Cell | denotes | cultured cells | http://purl.obolibrary.org/obo/CL:0000010 |