Statements (34)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
chromosomal band
|
| gptkbp:associatedWith |
gptkb:neuroblastoma
gptkb:1p36_deletion_syndrome distinct facial features intellectual disability neurodevelopmental disorders hearing loss seizures developmental delay cardiomyopathy |
| gptkbp:containsGene |
gptkb:CHD5
gptkb:TNFRSF8 gptkb:CAMTA1 gptkb:CASZ1 gptkb:GABRD gptkb:GNB1 gptkb:HSPG2 gptkb:KCNAB2 gptkb:PEX10 gptkb:PRDM16 gptkb:RERE gptkb:TP73 gptkb:UBE4B gptkb:CDC2L1 gptkb:KIF1B gptkb:MMP23B gptkb:TNFRSF1B SKI |
| gptkbp:deletionSyndrome |
gptkb:1p36_deletion_syndrome
|
| https://www.w3.org/2000/01/rdf-schema#label |
chromosome 1p36 region
|
| gptkbp:locatedOn |
chromosome 1
|
| gptkbp:locatedOnChromosome |
gptkb:1p36
|
| gptkbp:bfsParent |
gptkb:chromosome_1p36.23
|
| gptkbp:bfsLayer |
8
|