Statements (18)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
chromosomal band
|
| gptkbp:associatedWith |
genetic disorders
copy number variation chromosomal deletion chromosomal duplication |
| gptkbp:containsGene |
gptkb:ASXL1
gptkb:BCL2L1 gptkb:DNMT3B ID1 TPX2 |
| https://www.w3.org/2000/01/rdf-schema#label |
20q11.2 (human)
|
| gptkbp:locatedOn |
chromosome 20 (human)
|
| gptkbp:locatedOnChromosome |
gptkb:20q11.2
|
| gptkbp:notableFor |
frequent amplification in cancer
recurrent duplication in stem cell lines |
| gptkbp:organism |
gptkb:Homo_sapiens
|
| gptkbp:bfsParent |
gptkb:E2f1
|
| gptkbp:bfsLayer |
8
|