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DESCRIBE <http://purl.uniprot.org/SHA-384/459EBB21E3F6E3C5D39266D76B72192333DF301F4F7602F696812AD46BBE1831A09BE6170E038B4A98B65313E90FBE2F>
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http://purl.uniprot.org/SHA-384/459EBB21E3F6E3C5D39266D76B72192333DF301F4F7602F696812AD46BBE1831A09BE6170E038B4A98B65313E90FBE2F
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/459EBB21E3F6E3C5D39266D76B72192333DF301F4F7602F696812AD46BBE1831A09BE6170E038B4A98B65313E90FBE2F
http://www.w3.org/2000/01/rdf-schema#comment
"The point mutation c.-14C>T in the 5'-untranslated region of IFITM5 is responsible for osteogenesis imperfecta type V in Chinese patients."
xsd:string
http://purl.uniprot.org/uniprot/#_FD1BB78AD8A51765FDDC0F78EBFD08EE8D582DACC67A2B6C935B4629CA5567EC8BF2DD7E96EBE1C81B9F0EBA5EF530D7
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/459EBB21E3F6E3C5D39266D76B72192333DF301F4F7602F696812AD46BBE1831A09BE6170E038B4A98B65313E90FBE2F
http://purl.uniprot.org/uniprot/A6NNB3
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/459EBB21E3F6E3C5D39266D76B72192333DF301F4F7602F696812AD46BBE1831A09BE6170E038B4A98B65313E90FBE2F
http://purl.uniprot.org/uniprot/#_A6NNB3-mappedCitation-23977282
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/459EBB21E3F6E3C5D39266D76B72192333DF301F4F7602F696812AD46BBE1831A09BE6170E038B4A98B65313E90FBE2F