PubMed:10051007
Annnotations
PMID_GLOBAL
| Id | Subject | Object | Predicate | Lexical cue | mondo_id |
|---|---|---|---|---|---|
| T1 | 16-34 | DiseaseOrPhenotypicFeature | denotes | Huntington disease | 0007739 |
| T2 | 139-157 | DiseaseOrPhenotypicFeature | denotes | Huntington disease | 0007739 |
| T3 | 159-161 | DiseaseOrPhenotypicFeature | denotes | HD | 0007739 |
| T4 | 238-240 | DiseaseOrPhenotypicFeature | denotes | HD | 0007739 |
| T5 | 318-335 | DiseaseOrPhenotypicFeature | denotes | Alzheimer disease | 0004975|0007088 |
| T7 | 402-423 | DiseaseOrPhenotypicFeature | denotes | neurological diseases | 0005071 |
| T8 | 503-505 | DiseaseOrPhenotypicFeature | denotes | HD | 0007739 |
| T9 | 519-521 | DiseaseOrPhenotypicFeature | denotes | HD | 0007739 |
| T10 | 759-761 | DiseaseOrPhenotypicFeature | denotes | HD | 0007739 |
| T11 | 1071-1073 | DiseaseOrPhenotypicFeature | denotes | HD | 0007739 |
DisGeNET5_gene_disease
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| 10051007-0#62#78#gene348 | 62-78 | gene348 | denotes | apolipoprotein E |
| 10051007-0#16#34#diseaseC0020179 | 16-34 | diseaseC0020179 | denotes | Huntington disease |
| 10051007-2#0#16#gene348 | 247-263 | gene348 | denotes | Apolipoprotein E |
| 10051007-2#18#22#gene348 | 265-269 | gene348 | denotes | APOE |
| 10051007-2#71#88#diseaseC0002395 | 318-335 | diseaseC0002395 | denotes | Alzheimer disease |
| 62#78#gene34816#34#diseaseC0020179 | 10051007-0#62#78#gene348 | 10051007-0#16#34#diseaseC0020179 | associated_with | apolipoprotein E,Huntington disease |
| 0#16#gene34871#88#diseaseC0002395 | 10051007-2#0#16#gene348 | 10051007-2#71#88#diseaseC0002395 | associated_with | Apolipoprotein E,Alzheimer disease |
| 18#22#gene34871#88#diseaseC0002395 | 10051007-2#18#22#gene348 | 10051007-2#71#88#diseaseC0002395 | associated_with | APOE,Alzheimer disease |
NCBIDiseaseCorpus
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 16-34 | SpecificDisease:D006816 | denotes | Huntington disease |
| T2 | 139-157 | SpecificDisease:D006816 | denotes | Huntington disease |
| T3 | 159-161 | SpecificDisease:D006816 | denotes | HD |
| T4 | 238-240 | Modifier:D006816 | denotes | HD |
| T5 | 318-335 | SpecificDisease:D000544 | denotes | Alzheimer disease |
| T6 | 402-423 | DiseaseClass:D020271 | denotes | neurological diseases |
| T7 | 503-505 | Modifier:D006816 | denotes | HD |
| T8 | 519-521 | Modifier:D006816 | denotes | HD |
| T9 | 759-761 | SpecificDisease:D006816 | denotes | HD |
| T10 | 1050-1067 | DiseaseClass:D019636 | denotes | neurodegeneration |
| T11 | 1071-1073 | SpecificDisease:D006816 | denotes | HD |
PubmedHPO
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 318-335 | HP_0002511 | denotes | Alzheimer disease |
| T2 | 629-634 | HP_0000618 | denotes | blind |
| T3 | 1050-1067 | HP_0002180 | denotes | neurodegeneration |
DisGeNET
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T0 | 62-78 | gene:348 | denotes | apolipoprotein E |
| T1 | 16-34 | disease:C0020179 | denotes | Huntington disease |
| T2 | 265-269 | gene:348 | denotes | APOE |
| T3 | 318-335 | disease:C0002395 | denotes | Alzheimer disease |
| T4 | 247-263 | gene:348 | denotes | Apolipoprotein E |
| T5 | 318-335 | disease:C0002395 | denotes | Alzheimer disease |
| R1 | T0 | T1 | associated_with | apolipoprotein E,Huntington disease |
| R2 | T2 | T3 | associated_with | APOE,Alzheimer disease |
| R3 | T4 | T5 | associated_with | Apolipoprotein E,Alzheimer disease |
NCBI-Disease-Train
| Id | Subject | Object | Predicate | Lexical cue | database_id |
|---|---|---|---|---|---|
| T2715 | 16-34 | SpecificDisease | denotes | Huntington disease | D006816 |
| T2716 | 139-157 | SpecificDisease | denotes | Huntington disease | D006816 |
| T2717 | 159-161 | SpecificDisease | denotes | HD | D006816 |
| T2718 | 238-240 | Modifier | denotes | HD | D006816 |
| T2719 | 318-335 | SpecificDisease | denotes | Alzheimer disease | D000544 |
| T2720 | 402-423 | DiseaseClass | denotes | neurological diseases | D020271 |
| T2721 | 503-505 | Modifier | denotes | HD | D006816 |
| T2722 | 519-521 | Modifier | denotes | HD | D006816 |
| T2723 | 759-761 | SpecificDisease | denotes | HD | D006816 |
| T2724 | 1050-1067 | DiseaseClass | denotes | neurodegeneration | D019636 |
| T2725 | 1071-1073 | SpecificDisease | denotes | HD | D006816 |
NCBI-Disease-Corpus-All
| Id | Subject | Object | Predicate | Lexical cue | database_id |
|---|---|---|---|---|---|
| T2715 | 16-34 | SpecificDisease | denotes | Huntington disease | D006816 |
| T2716 | 139-157 | SpecificDisease | denotes | Huntington disease | D006816 |
| T2717 | 159-161 | SpecificDisease | denotes | HD | D006816 |
| T2718 | 238-240 | Modifier | denotes | HD | D006816 |
| T2719 | 318-335 | SpecificDisease | denotes | Alzheimer disease | D000544 |
| T2720 | 402-423 | DiseaseClass | denotes | neurological diseases | D020271 |
| T2721 | 503-505 | Modifier | denotes | HD | D006816 |
| T2722 | 519-521 | Modifier | denotes | HD | D006816 |
| T2723 | 759-761 | SpecificDisease | denotes | HD | D006816 |
| T2724 | 1050-1067 | DiseaseClass | denotes | neurodegeneration | D019636 |
| T2725 | 1071-1073 | SpecificDisease | denotes | HD | D006816 |
NCBI-Disease-Corpus-2stage-All
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 16-34 | SpecificDisease | denotes | Huntington disease |
| T2 | 139-157 | SpecificDisease | denotes | Huntington disease |
| T3 | 159-161 | SpecificDisease | denotes | HD |
| T4 | 238-240 | Modifier | denotes | HD |
| T5 | 318-335 | SpecificDisease | denotes | Alzheimer disease |
| T6 | 503-505 | Modifier | denotes | HD |
| T7 | 519-521 | Modifier | denotes | HD |
| T8 | 759-761 | SpecificDisease | denotes | HD |
| T9 | 1071-1073 | SpecificDisease | denotes | HD |
NCBI-Disease-Corpus-rezarta-All
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 16-34 | SpecificDisease | denotes | Huntington disease |
| T2 | 139-157 | SpecificDisease | denotes | Huntington disease |
| T3 | 159-161 | SpecificDisease | denotes | HD |
| T4 | 238-240 | Modifier | denotes | HD |
| T5 | 318-335 | SpecificDisease | denotes | Alzheimer disease |
| T6 | 503-505 | Modifier | denotes | HD |
| T7 | 519-521 | Modifier | denotes | HD |
| T8 | 759-761 | Modifier | denotes | HD |
| T9 | 1071-1073 | SpecificDisease | denotes | HD |
NCBI-Disease-Corpus-4oGuideline-All
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 16-34 | SpecificDisease | denotes | Huntington disease |
| T2 | 139-157 | SpecificDisease | denotes | Huntington disease |
| T3 | 159-161 | SpecificDisease | denotes | HD |
| T4 | 238-240 | SpecificDisease | denotes | HD |
| T5 | 318-335 | SpecificDisease | denotes | Alzheimer disease |
| T6 | 503-505 | SpecificDisease | denotes | HD |
| T7 | 519-521 | SpecificDisease | denotes | HD |
| T8 | 759-761 | Modifier | denotes | HD |
| T9 | 1071-1073 | SpecificDisease | denotes | HD |
NCBI-Disease-Corpus-Simple-All
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 16-34 | SpecificDisease | denotes | Huntington disease |
| T2 | 62-116 | CompositeMention | denotes | apolipoprotein E genotype and normal CAG repeat length |
| T3 | 139-162 | SpecificDisease | denotes | Huntington disease (HD) |
| T4 | 238-245 | SpecificDisease | denotes | HD gene |
| T5 | 247-279 | Modifier | denotes | Apolipoprotein E (APOE) genotype |
| T6 | 318-335 | SpecificDisease | denotes | Alzheimer disease |
| T7 | 351-360 | Modifier | denotes | APOE gene |
| T8 | 402-423 | DiseaseClass | denotes | neurological diseases |
| T9 | 453-466 | Modifier | denotes | APOE genotype |
| T10 | 503-510 | SpecificDisease | denotes | HD gene |
| T11 | 519-530 | SpecificDisease | denotes | HD patients |
| T12 | 738-758 | Modifier | denotes | maternally inherited |
| T13 | 759-761 | SpecificDisease | denotes | HD |
| T14 | 801-831 | Modifier | denotes | APOE epsilon2epsilon3 genotype |
| T15 | 968-982 | Modifier | denotes | APOE genotypes |
| T16 | 1050-1067 | DiseaseClass | denotes | neurodegeneration |
| T17 | 1071-1073 | SpecificDisease | denotes | HD |
| T18 | 1111-1126 | Modifier | denotes | gender specific |