Statements (17)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:gene
|
| gptkbp:alsoKnownAs |
gptkb:ERCC2
|
| gptkbp:associatedWith |
gptkb:Cockayne_syndrome
gptkb:trichothiodystrophy gptkb:xeroderma_pigmentosum |
| gptkbp:discoveredIn |
1990
|
| gptkbp:encodes |
gptkb:DNA_helicase_XPD
|
| gptkbp:Entrez_Gene_ID |
2068
|
| gptkbp:expressedIn |
gptkb:human
|
| gptkbp:HGNC_ID |
3433
|
| https://www.w3.org/2000/01/rdf-schema#label |
XPD
|
| gptkbp:involvedIn |
nucleotide excision repair
|
| gptkbp:locatedOnChromosome |
19q13.32
|
| gptkbp:OMIM |
126340
|
| gptkbp:UniProtID |
P18074
|
| gptkbp:bfsParent |
gptkb:ISO_4217
|
| gptkbp:bfsLayer |
6
|