PubMed:15987957 / 0-161
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 |
ICD10
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 152-160 | 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 |
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 |
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 |
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 |
HP-phenotype
Id | Subject | Object | Predicate | Lexical cue | hp_id |
---|---|---|---|---|---|
T1 | 152-160 | Phenotype | denotes | myopathy | HP:0003198 |
NCBITAXON
Id | Subject | Object | Predicate | Lexical cue | db_id |
---|---|---|---|---|---|
T1 | 120-125 | OrganismTaxon | denotes | human | 9606 |