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- NP899537.RASM8b5I1wQgg9g9JN0W--Nb-tjSz4FWeXC3dJIyGnIr4130_assertion type Assertion NP899537.RASM8b5I1wQgg9g9JN0W--Nb-tjSz4FWeXC3dJIyGnIr4130_head.
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- NP899537.RASM8b5I1wQgg9g9JN0W--Nb-tjSz4FWeXC3dJIyGnIr4130_assertion SIO_000772 17027633 NP899537.RASM8b5I1wQgg9g9JN0W--Nb-tjSz4FWeXC3dJIyGnIr4130_provenance.
- NP899537.RASM8b5I1wQgg9g9JN0W--Nb-tjSz4FWeXC3dJIyGnIr4130_assertion evidence source_evidence_literature NP899537.RASM8b5I1wQgg9g9JN0W--Nb-tjSz4FWeXC3dJIyGnIr4130_provenance.
- NP899537.RASM8b5I1wQgg9g9JN0W--Nb-tjSz4FWeXC3dJIyGnIr4130_assertion description "[Cardiac troponin I (cTnI) mutations have been linked to the development of restrictive cardiomyopathy (RCM) in human patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP899537.RASM8b5I1wQgg9g9JN0W--Nb-tjSz4FWeXC3dJIyGnIr4130_provenance.