PubMed:1674745 / 61-183
Annnotations
sentences
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T2 | 0-122 | Sentence | denotes | Homozygosity for two rare point mutations in the apolipoprotein E gene combined with severe type III hyperlipoproteinemia. |
| T2 | 0-122 | Sentence | denotes | Homozygosity for two rare point mutations in the apolipoprotein E gene combined with severe type III hyperlipoproteinemia. |
DisGeNET5_gene_disease
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| 1674745-0#110#126#gene348 | 49-65 | gene348 | denotes | apolipoprotein E |
| 1674745-0#153#182#diseaseC0020479 | 92-121 | diseaseC0020479 | denotes | type III hyperlipoproteinemia |
| 110#126#gene348153#182#diseaseC0020479 | 1674745-0#110#126#gene348 | 1674745-0#153#182#diseaseC0020479 | associated_with | apolipoprotein E,type III hyperlipoproteinemia |
PubCasesHPO
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| TI1 | 101-121 | HP:0010980 | denotes | hyperlipoproteinemia |
DisGeNET
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 92-121 | disease:C0020479 | denotes | type III hyperlipoproteinemia |
| T2 | 49-65 | gene:348 | denotes | apolipoprotein E |
| T3 | 92-121 | disease:C0020479 | denotes | type III hyperlipoproteinemia |
| R2 | T2 | T3 | associated_with | apolipoprotein E,type III hyperlipoproteinemia |
mondo_disease
| Id | Subject | Object | Predicate | Lexical cue | mondo_id |
|---|---|---|---|---|---|
| T1 | 101-121 | Disease | denotes | hyperlipoproteinemia | http://purl.obolibrary.org/obo/MONDO_0037748 |
HP-phenotype
| Id | Subject | Object | Predicate | Lexical cue | hp_id |
|---|---|---|---|---|---|
| T1 | 101-121 | Phenotype | denotes | hyperlipoproteinemia | HP:0010980 |