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- NP578458.RAl-PR-RIAuC50r6aOI4xktySEvP692lw4JBnBjLMaFkU130_assertion type Assertion NP578458.RAl-PR-RIAuC50r6aOI4xktySEvP692lw4JBnBjLMaFkU130_head.
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- NP578458.RAl-PR-RIAuC50r6aOI4xktySEvP692lw4JBnBjLMaFkU130_assertion wasDerivedFrom befree-2016 NP578458.RAl-PR-RIAuC50r6aOI4xktySEvP692lw4JBnBjLMaFkU130_provenance.
- NP578458.RAl-PR-RIAuC50r6aOI4xktySEvP692lw4JBnBjLMaFkU130_assertion SIO_000772 17094098 NP578458.RAl-PR-RIAuC50r6aOI4xktySEvP692lw4JBnBjLMaFkU130_provenance.
- NP578458.RAl-PR-RIAuC50r6aOI4xktySEvP692lw4JBnBjLMaFkU130_assertion evidence source_evidence_literature NP578458.RAl-PR-RIAuC50r6aOI4xktySEvP692lw4JBnBjLMaFkU130_provenance.
- NP578458.RAl-PR-RIAuC50r6aOI4xktySEvP692lw4JBnBjLMaFkU130_assertion description "[Transthyretin amyloid neuropathy of type 1 (Swedish-Portuguese type) is an autosomally inherited progressive disease with a Val30Met mutation, causing generalized sensory-motor polyneuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP578458.RAl-PR-RIAuC50r6aOI4xktySEvP692lw4JBnBjLMaFkU130_provenance.