genomicAlteration
P97055
predicate
Indicates a relationship where an entity has undergone a change or mutation in its genetic material compared to a reference genome.
Observed surface forms (3)
| Surface form | Occurrences |
|---|---|
| oncogenicAlteration | 7 |
| chromosomeVariation | 2 |
| pathogenicVariantType | 1 |
Sample triples (12)
| Subject | Object |
|---|---|
| ERBB2 | gene amplification ⓘ |
| ERBB2 | overexpression ⓘ |
| Gossypium | diploid species via predicate surface "chromosomeVariation" ⓘ |
| Gossypium | allotetraploid species via predicate surface "chromosomeVariation" ⓘ |
|
chromosome 9 open reading frame 72
surface form:
C9orf72
|
large hexanucleotide repeat expansion via predicate surface "pathogenicVariantType" ⓘ |
| EGFR | gene amplification via predicate surface "oncogenicAlteration" ⓘ |
| EGFR | activating point mutation via predicate surface "oncogenicAlteration" ⓘ |
| EGFR | exon 19 deletion mutation via predicate surface "oncogenicAlteration" ⓘ |
| EGFR | L858R point mutation in exon 21 via predicate surface "oncogenicAlteration" ⓘ |
| EGFR | T790M resistance mutation via predicate surface "oncogenicAlteration" ⓘ |
| EGFR | extracellular domain mutation via predicate surface "oncogenicAlteration" ⓘ |
| EGFR | EGFRvIII deletion mutant via predicate surface "oncogenicAlteration" NERFINISHED ⓘ |