PubMed:1719554
Annnotations
PMID_GLOBAL
| Id | Subject | Object | Predicate | Lexical cue | mondo_id |
|---|---|---|---|---|---|
| T1 | 103-111 | DiseaseOrPhenotypicFeature | denotes | syndrome | 0002254 |
| T2 | 165-168 | DiseaseOrPhenotypicFeature | denotes | can | 0012833 |
| T3 | 316-318 | DiseaseOrPhenotypicFeature | denotes | BP | 0022022 |
| T4 | 346-348 | DiseaseOrPhenotypicFeature | denotes | BP | 0022022 |
| T5 | 656-670 | DiseaseOrPhenotypicFeature | denotes | Laron syndrome | 0009877 |
DisGeNET
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T0 | 275-278 | gene:2690 | denotes | GHR |
| T1 | 465-473 | disease:C0013336 | denotes | dwarfism |
| R1 | T0 | T1 | associated_with | GHR,dwarfism |
PubmedHPO
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 465-473 | HP_0003510 | denotes | dwarfism |
DisGeNET5_variant_disease
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| 1719554-3#101#139#geners751687643 | 576-614 | geners751687643 | denotes | phenylalanine by serine at position 96 |
| 1719554-3#181#195#diseaseC0271568 | 656-670 | diseaseC0271568 | denotes | Laron syndrome |
| 101#139#geners751687643181#195#diseaseC0271568 | 1719554-3#101#139#geners751687643 | 1719554-3#181#195#diseaseC0271568 | associated_with | phenylalanine by serine at position 96,Laron syndrome |
DisGeNET5_gene_disease
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| 1719554-2#68#71#gene2690 | 275-278 | gene2690 | denotes | GHR |
| 1719554-2#86#88#gene2688 | 293-295 | gene2688 | denotes | GH |
| 1719554-2#258#266#diseaseC0013336 | 465-473 | diseaseC0013336 | denotes | dwarfism |
| 68#71#gene2690258#266#diseaseC0013336 | 1719554-2#68#71#gene2690 | 1719554-2#258#266#diseaseC0013336 | associated_with | GHR,dwarfism |
| 86#88#gene2688258#266#diseaseC0013336 | 1719554-2#86#88#gene2688 | 1719554-2#258#266#diseaseC0013336 | associated_with | GH,dwarfism |