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DESCRIBE <http://purl.uniprot.org/SHA-384/F276DC9AB5DE7934283C7D04D7776CD81223DA4D6B127665C5194B4485EC81C1A48C1BB8710473B90EF262EEBDB84B9C>
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http://purl.uniprot.org/SHA-384/F276DC9AB5DE7934283C7D04D7776CD81223DA4D6B127665C5194B4485EC81C1A48C1BB8710473B90EF262EEBDB84B9C
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/F276DC9AB5DE7934283C7D04D7776CD81223DA4D6B127665C5194B4485EC81C1A48C1BB8710473B90EF262EEBDB84B9C
http://www.w3.org/2000/01/rdf-schema#comment
"The present study reports a novel mutation c.718C>G; p. (Arg240Gly) in the melanogenesis associated transcription factor gene in Han people with hearing loss."
xsd:string
http://purl.uniprot.org/uniprot/#_A898A414A872E09B4FD887719513012D0E91ABC1A1ED4321FEE0533CB13215671108BE30AA2DCB3DA44FD35088DC7D0F
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/F276DC9AB5DE7934283C7D04D7776CD81223DA4D6B127665C5194B4485EC81C1A48C1BB8710473B90EF262EEBDB84B9C
http://purl.uniprot.org/uniprot/Q8IUH6
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/F276DC9AB5DE7934283C7D04D7776CD81223DA4D6B127665C5194B4485EC81C1A48C1BB8710473B90EF262EEBDB84B9C
http://purl.uniprot.org/uniprot/#_Q8IUH6-mappedCitation-29484430
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/F276DC9AB5DE7934283C7D04D7776CD81223DA4D6B127665C5194B4485EC81C1A48C1BB8710473B90EF262EEBDB84B9C