PubMed:15987957 / 0-235
Annnotations
Glycan-Motif
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 43-62 | https://glytoucan.org/Structures/Glycans/G64581RP | denotes | N-acetylglucosamine |
GlyCosmos6-Glycan-Motif-Image
| Id | Subject | Object | Predicate | Lexical cue | image |
|---|---|---|---|---|---|
| T1 | 43-62 | Glycan_Motif | denotes | N-acetylglucosamine | https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G64581RP |
GlyCosmos6-Glycan-Motif-Structure
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 43-62 | https://glytoucan.org/Structures/Glycans/G64581RP | denotes | N-acetylglucosamine |
sentences
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| TextSentencer_T1 | 0-161 | Sentence | denotes | Use of a cell-free system to determine UDP-N-acetylglucosamine 2-epimerase and N-acetylmannosamine kinase activities in human hereditary inclusion body myopathy. |
| T1 | 0-161 | Sentence | denotes | Use of a cell-free system to determine UDP-N-acetylglucosamine 2-epimerase and N-acetylmannosamine kinase activities in human hereditary inclusion body myopathy. |
| T1 | 0-161 | Sentence | denotes | Use of a cell-free system to determine UDP-N-acetylglucosamine 2-epimerase and N-acetylmannosamine kinase activities in human hereditary inclusion body myopathy. |
GlycoBiology-GDGDB
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| _T17 | 126-160 | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00385 | denotes | hereditary inclusion body myopathy |
| _T18 | 162-196 | http://acgg.asia/db/diseases/gdgdb?con_ui=CON00385 | denotes | Hereditary inclusion body myopathy |
ICD10
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 152-160 | http://purl.bioontology.org/ontology/ICD10/G72.9 | denotes | myopathy |
| T2 | 188-196 | http://purl.bioontology.org/ontology/ICD10/G72.9 | denotes | myopathy |
uniprot-human
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 63-80 | http://www.uniprot.org/uniprot/P51606 | denotes | 2-epimerase and N |
| T2 | 79-105 | http://www.uniprot.org/uniprot/F5H499 | denotes | N-acetylmannosamine kinase |
uniprot-mouse
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 79-105 | http://www.uniprot.org/uniprot/Q91WG8 | denotes | N-acetylmannosamine kinase |
GlycoBiology-NCBITAXON
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 210-219 | http://purl.bioontology.org/ontology/NCBITAXON/150701 | denotes | autosomal |
GO-BP
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 79-116 | http://purl.obolibrary.org/obo/GO_0009384 | denotes | N-acetylmannosamine kinase activities |
| T2 | 99-116 | http://purl.obolibrary.org/obo/GO_0033674 | denotes | kinase activities |
| T3 | 99-116 | http://purl.obolibrary.org/obo/GO_0016301 | denotes | kinase activities |
GO-CC
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 9-13 | http://purl.obolibrary.org/obo/GO_0005623 | denotes | cell |
| T8 | 137-151 | http://purl.obolibrary.org/obo/GO_0016234 | denotes | inclusion body |
| T9 | 173-187 | http://purl.obolibrary.org/obo/GO_0016234 | denotes | inclusion body |
| T10 | 210-219 | http://purl.obolibrary.org/obo/GO_0030849 | denotes | autosomal |
EDAM-topics
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 120-125 | http://edamontology.org/topic_2815 | denotes | human |
NGLY1-deficiency
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| PD-NGLY1-deficiency-B_T1 | 43-62 | chem:24139 | denotes | N-acetylglucosamine |
DisGeNET5_gene_disease
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| 15987957-1#0#34#diseaseC1853926 | 162-196 | diseaseC1853926 | denotes | Hereditary inclusion body myopathy |
| 15987957-1#36#40#diseaseC1853926 | 198-202 | diseaseC1853926 | denotes | HIBM |
mondo_disease
| Id | Subject | Object | Predicate | Lexical cue | mondo_id |
|---|---|---|---|---|---|
| T1 | 126-160 | Disease | denotes | hereditary inclusion body myopathy | http://purl.obolibrary.org/obo/MONDO_0007827 |
| T2 | 162-196 | Disease | denotes | Hereditary inclusion body myopathy | http://purl.obolibrary.org/obo/MONDO_0007827 |
| T3 | 198-202 | Disease | denotes | HIBM | http://purl.obolibrary.org/obo/MONDO_0007827 |
HP-phenotype
| Id | Subject | Object | Predicate | Lexical cue | hp_id |
|---|---|---|---|---|---|
| T1 | 152-160 | Phenotype | denotes | myopathy | HP:0003198 |
| T2 | 188-196 | Phenotype | denotes | myopathy | HP:0003198 |
NCBITAXON
| Id | Subject | Object | Predicate | Lexical cue | db_id |
|---|---|---|---|---|---|
| T1 | 120-125 | OrganismTaxon | denotes | human | 9606 |