Statements (12)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
chromosomal band
|
| gptkbp:associatedWith |
gptkb:Fanconi_anemia
gptkb:Gorlin_syndrome Basal cell nevus syndrome |
| gptkbp:containsGene |
gptkb:FANCC
gptkb:PTCH1 |
| gptkbp:genomicCoordinates(hg38) |
chr9:95,000,001-100,000,000
|
| https://www.w3.org/2000/01/rdf-schema#label |
chromosome 9q22.3
|
| gptkbp:locatedOn |
gptkb:chromosome_9
|
| gptkbp:locatedOnChromosome |
9q22.3
|
| gptkbp:bfsParent |
gptkb:Fanconi_anemia_group_C_protein
|
| gptkbp:bfsLayer |
7
|