PubMed:18490429 / 386-523
Annnotations
sentences
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| TextSentencer_T4 | 0-137 | Sentence | denotes | Mutations in human POMT1 and POMT2 cause a group of congenital muscular dystrophies due to reduced O-glycosylation of alpha-dystroglycan. |
| T4 | 0-137 | Sentence | denotes | Mutations in human POMT1 and POMT2 cause a group of congenital muscular dystrophies due to reduced O-glycosylation of alpha-dystroglycan. |
| T4 | 0-137 | Sentence | denotes | Mutations in human POMT1 and POMT2 cause a group of congenital muscular dystrophies due to reduced O-glycosylation of alpha-dystroglycan. |
DisGeNET
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T2 | 118-136 | gene:1605 | denotes | alpha-dystroglycan |
| T3 | 63-83 | disease:C0026850 | denotes | muscular dystrophies |
| T4 | 29-34 | gene:29954 | denotes | POMT2 |
| T5 | 63-83 | disease:C0026850 | denotes | muscular dystrophies |
| T6 | 19-24 | gene:10585 | denotes | POMT1 |
| T7 | 63-83 | disease:C0026850 | denotes | muscular dystrophies |
| R2 | T2 | T3 | associated_with | alpha-dystroglycan,muscular dystrophies |
| R3 | T4 | T5 | associated_with | POMT2,muscular dystrophies |
| R4 | T6 | T7 | associated_with | POMT1,muscular dystrophies |
GlycoBiology-GDGDB
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| _T4 | 19-24 | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00376 | denotes | POMT1 |
| _T5 | 29-34 | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00376 | denotes | POMT2 |
| _T10 | 52-83 | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00381 | denotes | congenital muscular dystrophies |
| _T11 | 52-83 | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00383 | denotes | congenital muscular dystrophies |
ICD10
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 63-83 | http://purl.bioontology.org/ontology/ICD10/G71.0 | denotes | muscular dystrophies |
uniprot-human
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T3 | 29-34 | http://www.uniprot.org/uniprot/Q9UKY4 | denotes | POMT2 |
| T5 | 19-24 | http://www.uniprot.org/uniprot/Q9NX32 | denotes | POMT1 |
| T7 | 124-136 | http://www.uniprot.org/uniprot/Q14118 | denotes | dystroglycan |
uniprot-mouse
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 124-136 | http://www.uniprot.org/uniprot/Q62165 | denotes | dystroglycan |
GlycoBiology-NCBITAXON
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T3 | 43-48 | http://purl.bioontology.org/ontology/STY/T096 | denotes | group |
GO-BP
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T8 | 101-114 | http://purl.obolibrary.org/obo/GO_0070085 | denotes | glycosylation |
DisGeNET5_gene_disease
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| 18490429-3#29#34#gene29954 | 29-34 | gene29954 | denotes | POMT2 |
| 18490429-3#118#136#gene1605 | 118-136 | gene1605 | denotes | alpha-dystroglycan |
| 18490429-3#63#83#diseaseC0026850 | 63-83 | diseaseC0026850 | denotes | muscular dystrophies |
| 29#34#gene2995463#83#diseaseC0026850 | 18490429-3#29#34#gene29954 | 18490429-3#63#83#diseaseC0026850 | associated_with | POMT2,muscular dystrophies |
| 118#136#gene160563#83#diseaseC0026850 | 18490429-3#118#136#gene1605 | 18490429-3#63#83#diseaseC0026850 | associated_with | alpha-dystroglycan,muscular dystrophies |
HP-phenotype
| Id | Subject | Object | Predicate | Lexical cue | hp_id |
|---|---|---|---|---|---|
| T1 | 52-83 | Phenotype | denotes | congenital muscular dystrophies | HP:0003560 |
mondo_disease
| Id | Subject | Object | Predicate | Lexical cue | mondo_id |
|---|---|---|---|---|---|
| T2 | 52-83 | Disease | denotes | congenital muscular dystrophies | http://purl.obolibrary.org/obo/MONDO_0019950 |
NCBITAXON
| Id | Subject | Object | Predicate | Lexical cue | db_id |
|---|---|---|---|---|---|
| T1 | 13-18 | OrganismTaxon | denotes | human | 9606 |