OMIMID
P68676
predicate
Indicates that an entity (typically a gene or disease) is associated with a specific OMIM (Online Mendelian Inheritance in Man) identifier in the OMIM database.
All labels observed (2)
| Label | Occurrences |
|---|---|
| OMIMID canonical | 7 |
| hasOMIMID | 2 |
Description generation (PDg)
The one-sentence description above was generated by prompting gpt-5.1 with the predicate name and this instruction.
Instruction
Given a predicate that represents a relationship or action between entities, generate a one-sentence description explaining its meaning. # Instructions Focus on describing the relationship, not the entities themselves. # Response Format Begin the description with \' Indicates...\'
Input
Predicate: OMIMID
Generated description
Indicates that an entity (typically a gene or disease) is associated with a specific OMIM (Online Mendelian Inheritance in Man) identifier in the OMIM database.
Sample triples (9)
| Subject | Object |
|---|---|
| C9orf72 | 614260 ⓘ |
| Dravet syndrome | 607208 via predicate surface "hasOMIMID" ⓘ |
|
SMN1 gene
surface form:
SMN1
|
600354 ⓘ |
| 5q13 (SMN1) | 600354 ⓘ |
| Vrolik syndrome | 166210 via predicate surface "hasOMIMID" ⓘ |
|
HTT gene
surface form:
HTT
|
613004 ⓘ |
| SCN1A | 182389 ⓘ |
| Angelman syndrome | 105830 ⓘ |
| Krabbe disease | 245200 ⓘ |