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DESCRIBE <http://purl.uniprot.org/SHA-384/8CB6E218FDEF5124E1E7FEC58DC4499FC23B75862E364CFEC910330ED7E8FBF61283502DA3D615763D912C46B304B970>
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http://purl.uniprot.org/SHA-384/8CB6E218FDEF5124E1E7FEC58DC4499FC23B75862E364CFEC910330ED7E8FBF61283502DA3D615763D912C46B304B970
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/8CB6E218FDEF5124E1E7FEC58DC4499FC23B75862E364CFEC910330ED7E8FBF61283502DA3D615763D912C46B304B970
http://www.w3.org/2000/01/rdf-schema#comment
"Mutations in the HSP47 and FKBP65 produce a moderately severe form of Osteogenesis imperfect."
xsd:string
http://purl.uniprot.org/uniprot/#_F77FB47DDC8D5E2812A83697BFFB439118748314D7B7F7489D20D46B6C773823B8EBA5C0DC68F0A0375AE1303E9B655A
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/8CB6E218FDEF5124E1E7FEC58DC4499FC23B75862E364CFEC910330ED7E8FBF61283502DA3D615763D912C46B304B970
http://purl.uniprot.org/uniprot/P50454
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/8CB6E218FDEF5124E1E7FEC58DC4499FC23B75862E364CFEC910330ED7E8FBF61283502DA3D615763D912C46B304B970
http://purl.uniprot.org/uniprot/#_P50454-mappedCitation-25510505
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/8CB6E218FDEF5124E1E7FEC58DC4499FC23B75862E364CFEC910330ED7E8FBF61283502DA3D615763D912C46B304B970