PubMed:18827003
Annnotations
PMID_GLOBAL
Id | Subject | Object | Predicate | Lexical cue | mondo_id |
---|---|---|---|---|---|
T1 | 194-205 | DiseaseOrPhenotypicFeature | denotes | sensitivity | 0000605 |
T2 | 250-265 | DiseaseOrPhenotypicFeature | denotes | cortisol excess | 0018912 |
T3 | 487-503 | DiseaseOrPhenotypicFeature | denotes | hypersensitivity | 0000605|0005271 |
T5 | 1041-1054 | DiseaseOrPhenotypicFeature | denotes | mammary tumor | 0007254 |
T6 | 1743-1750 | DiseaseOrPhenotypicFeature | denotes | obesity | 0011122 |
T7 | 1752-1764 | DiseaseOrPhenotypicFeature | denotes | hypertension | 0005044 |
T8 | 1798-1816 | DiseaseOrPhenotypicFeature | denotes | metabolic syndrome | 0004955 |
tmVarCorpus
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 558-597 | DNAMutation:c|SUB|G|1201|C | denotes | (G --> C) substitution at position 1201 |
T2 | 845-850 | ProteinMutation:p|SUB|D|401|H | denotes | D401H |
T3 | 935-940 | ProteinMutation:p|SUB|D|401|H | denotes | D401H |
T4 | 1299-1304 | ProteinMutation:p|SUB|D|401|H | denotes | D401H |
T5 | 1601-1606 | ProteinMutation:p|SUB|D|401|H | denotes | D401H |
T6 | 1701-1706 | ProteinMutation:p|SUB|D|401|H | denotes | D401H |