ID   HPSI0616i-giql_1
AC   CVCL_LL72
SY   WTSIi506-B; WTSIi577-A
DR   BioSamples; SAMEA103884210
DR   ECACC; 77650653
DR   HipSci; HPSI0616i-giql_1
DR   hPSCreg; WTSIi506-B
DR   Wikidata; Q54891198
CC   From: Cambridge BioResource; Cambridge; United Kingdom.
CC   From: Wellcome Trust Sanger Institute; Hinxton; 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_LL73 ! HPSI0616i-giql_5
SX   Female
AG   55-59Y
CA   Induced pluripotent stem cell
DT   Created: 15-11-17; Last updated: 29-06-23; Version: 9
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