DESCRIBE <http://purl.uniprot.org/SHA-384/C073C467048F241C72B64573C67CFA00C65D903DFD1D90183B1AAD06286C3B2DAD1095D692BBFBA01ECB3AF738964BC6>

Subject	Predicate	Object
http://purl.uniprot.org/SHA-384/C073C467048F241C72B64573C67CFA00C65D903DFD1D90183B1AAD06286C3B2DAD1095D692BBFBA01ECB3AF738964BC6	http://www.w3.org/1999/02/22-rdf-syntax-ns#type	http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/C073C467048F241C72B64573C67CFA00C65D903DFD1D90183B1AAD06286C3B2DAD1095D692BBFBA01ECB3AF738964BC6	http://www.w3.org/2000/01/rdf-schema#comment	"Genetic analysis of ACVR1 identified the recurrent allelic variant c.617 G>A; p.R206H in 12 of 14 Fibrodysplasia Ossificans Progressiva (FOP)patients. One of the remaining patients had a previously reported allele c.1067G>A; p.G356D in the 9th exon and the second allele c.983G>A; p.G328E in the 8th exon of ACVR1."xsd:string
http://purl.uniprot.org/uniprot/#_0AA7D3670AA07EFC9B88FCBDED98CA61825D79802ABE61EE1E908BD5C79B5648AC8A7C10094F664370B8999AF5CCEE7B	http://www.w3.org/1999/02/22-rdf-syntax-ns#subject	http://purl.uniprot.org/SHA-384/C073C467048F241C72B64573C67CFA00C65D903DFD1D90183B1AAD06286C3B2DAD1095D692BBFBA01ECB3AF738964BC6
http://purl.uniprot.org/uniprot/Q53SF4	http://purl.uniprot.org/core/mappedAnnotation	http://purl.uniprot.org/SHA-384/C073C467048F241C72B64573C67CFA00C65D903DFD1D90183B1AAD06286C3B2DAD1095D692BBFBA01ECB3AF738964BC6
http://purl.uniprot.org/uniprot/#_Q53SF4-mappedCitation-26058333	http://purl.uniprot.org/core/mappedAnnotation	http://purl.uniprot.org/SHA-384/C073C467048F241C72B64573C67CFA00C65D903DFD1D90183B1AAD06286C3B2DAD1095D692BBFBA01ECB3AF738964BC6