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http://purl.uniprot.org/SHA-384/7015D3CFCDF0BFE361C6611A81861A4C12451B4A74AB056A71DBA8119559B95C7C4771B3109FAFD5198D0806A62307A9http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/7015D3CFCDF0BFE361C6611A81861A4C12451B4A74AB056A71DBA8119559B95C7C4771B3109FAFD5198D0806A62307A9http://www.w3.org/2000/01/rdf-schema#comment"Fibrodysplasia ossificans progressiva (FOP) syndrome is caused by mutation of the gene ACVR1. Developed is a simplified one-step procedure by simultaneously introducing reprogramming and gene-editing components into human fibroblasts derived from patient with FOP. The one-step-mediated ALK2 gene-corrected induced pluripotent stem cells restored global gene expression pattern."xsd:string
http://purl.uniprot.org/uniprot/#_EAC9426E1D92FE2A38FB499EE114DE9DC05B80B723E4EFE82F81C05EA2BF45B0018BBD243AA4618017926B884D308CFEhttp://www.w3.org/1999/02/22-rdf-syntax-ns#subjecthttp://purl.uniprot.org/SHA-384/7015D3CFCDF0BFE361C6611A81861A4C12451B4A74AB056A71DBA8119559B95C7C4771B3109FAFD5198D0806A62307A9
http://purl.uniprot.org/uniprot/Q53SF4http://purl.uniprot.org/core/mappedAnnotationhttp://purl.uniprot.org/SHA-384/7015D3CFCDF0BFE361C6611A81861A4C12451B4A74AB056A71DBA8119559B95C7C4771B3109FAFD5198D0806A62307A9
http://purl.uniprot.org/uniprot/#_Q53SF4-mappedCitation-27256111http://purl.uniprot.org/core/mappedAnnotationhttp://purl.uniprot.org/SHA-384/7015D3CFCDF0BFE361C6611A81861A4C12451B4A74AB056A71DBA8119559B95C7C4771B3109FAFD5198D0806A62307A9