PubMed:2019586 / 372-561
Annnotations
GlyCosmos6-Glycan-Motif-Image
| Id | Subject | Object | Predicate | Lexical cue | image |
|---|---|---|---|---|---|
| T10 | 24-33 | Glycan_Motif | denotes | sulfatide | https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G95090DW|https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G72548RZ|https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G40843KY |
GlyCosmos6-Glycan-Motif-Structure
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T10 | 24-33 | https://glytoucan.org/Structures/Glycans/G40843KY | denotes | sulfatide |
| T11 | 24-33 | https://glytoucan.org/Structures/Glycans/G72548RZ | denotes | sulfatide |
| T12 | 24-33 | https://glytoucan.org/Structures/Glycans/G95090DW | denotes | sulfatide |
sentences
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| TextSentencer_T5 | 0-189 | Sentence | denotes | A genetic defect in the sulfatide activator results in a metabolic disorder similar to classical metachromatic leukodystrophy, which is itself caused by a genetic defect in arylsulfatase A. |
| T5 | 0-189 | Sentence | denotes | A genetic defect in the sulfatide activator results in a metabolic disorder similar to classical metachromatic leukodystrophy, which is itself caused by a genetic defect in arylsulfatase A. |
PubmedHPO
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 57-75 | HP_0001939 | denotes | metabolic disorder |
| T2 | 111-125 | HP_0002415 | denotes | leukodystrophy |
PubCasesHPO
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| AB1 | 111-125 | HP:0002415 | denotes | leukodystrophy |
PubCasesORDO
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| AB1 | 97-125 | ORDO:512 | denotes | metachromatic leukodystrophy |
mondo_disease
| Id | Subject | Object | Predicate | Lexical cue | mondo_id |
|---|---|---|---|---|---|
| T1 | 57-75 | Disease | denotes | metabolic disorder | http://purl.obolibrary.org/obo/MONDO_0005066 |
| T2 | 97-125 | Disease | denotes | metachromatic leukodystrophy | http://purl.obolibrary.org/obo/MONDO_0009591|http://purl.obolibrary.org/obo/MONDO_0018868 |
HP-phenotype
| Id | Subject | Object | Predicate | Lexical cue | hp_id |
|---|---|---|---|---|---|
| T1 | 111-125 | Phenotype | denotes | leukodystrophy | HP:0002415 |