DESCRIBE <http://purl.uniprot.org/SHA-384/DF169014871635637852CABD17A86F15844471933E22D5F945D0775F5BFAFFBC5B417D39BBB47CEE48169A2C3A113E57>

Subject	Predicate	Object
http://purl.uniprot.org/SHA-384/DF169014871635637852CABD17A86F15844471933E22D5F945D0775F5BFAFFBC5B417D39BBB47CEE48169A2C3A113E57	http://www.w3.org/1999/02/22-rdf-syntax-ns#type	http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/DF169014871635637852CABD17A86F15844471933E22D5F945D0775F5BFAFFBC5B417D39BBB47CEE48169A2C3A113E57	http://www.w3.org/2000/01/rdf-schema#comment	"s clinicians consider the presence or absence of conditions allelic at OFD1 PCD should be considered part of the spectrum of OFD1-related disorders. Understanding the OFD1-related disease spectrum may allow for more focused genetic testing and more timely management of treatable sequelae."xsd:string
http://purl.uniprot.org/uniprot/#_6A0941704A0927179D61E6F7754CDA75E36A92286AAC3E5324F29061BFF552C9A0B26830C4305174C7120F622055DB4F	http://www.w3.org/1999/02/22-rdf-syntax-ns#subject	http://purl.uniprot.org/SHA-384/DF169014871635637852CABD17A86F15844471933E22D5F945D0775F5BFAFFBC5B417D39BBB47CEE48169A2C3A113E57
http://purl.uniprot.org/uniprot/A8K2T9	http://purl.uniprot.org/core/mappedAnnotation	http://purl.uniprot.org/SHA-384/DF169014871635637852CABD17A86F15844471933E22D5F945D0775F5BFAFFBC5B417D39BBB47CEE48169A2C3A113E57
http://purl.uniprot.org/uniprot/#_A8K2T9-mappedCitation-31373179	http://purl.uniprot.org/core/mappedAnnotation	http://purl.uniprot.org/SHA-384/DF169014871635637852CABD17A86F15844471933E22D5F945D0775F5BFAFFBC5B417D39BBB47CEE48169A2C3A113E57