ID   HPSI0616i-kulz_6
AC   CVCL_IZ28
SY   WTSIi456-B; WTSIi523-A
DR   BioSamples; SAMEA17506918
DR   ECACC; 77650582
DR   HipSci; HPSI0616i-kulz_6
DR   hPSCreg; WTSIi456-B
DR   Wikidata; Q54891209
CC   From: Wellcome Trust Sanger Institute; Hinxton; United Kingdom.
CC   From: Cambridge BioResource; Cambridge; United Kingdom.
CC   Omics: Deep exome analysis.
CC   Omics: Transcriptome analysis by RNAseq.
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C103172; Congenital bleeding disorder
DI   ORDO; Orphanet_248308; Rare hemorrhagic disorder
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_IZ27 ! HPSI0616i-kulz_3
SX   Female
AG   60-64Y
CA   Induced pluripotent stem cell
DT   Created: 15-05-17; Last updated: 29-06-23; Version: 10
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