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An Entity of Type :
wikibase:Statement
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BestRank
Statement
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BestRank
Statement
OpenCitations bibliographic resource ID
4007479
psn:P3181
https://w3id.org/oc/corpus/br/4007479
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wdref:4f4c256dacdfbcd731a15aee576904aae47f0d1f
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OpenCitations bibliographic resource ID
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Congenital myopathy with nemaline rods and cap structures caused by a mutation in the beta-tropomyosin gene (TPM2)
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