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- NP583192.RA_dLDXxVbpXgIRp21T0rdhvDIjx1jEXhJX5pWXZhKu68130_assertion type Assertion NP583192.RA_dLDXxVbpXgIRp21T0rdhvDIjx1jEXhJX5pWXZhKu68130_head.
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- NP583192.RA_dLDXxVbpXgIRp21T0rdhvDIjx1jEXhJX5pWXZhKu68130_assertion wasDerivedFrom befree-20150227 NP583192.RA_dLDXxVbpXgIRp21T0rdhvDIjx1jEXhJX5pWXZhKu68130_provenance.
- NP583192.RA_dLDXxVbpXgIRp21T0rdhvDIjx1jEXhJX5pWXZhKu68130_assertion SIO_000772 17434305 NP583192.RA_dLDXxVbpXgIRp21T0rdhvDIjx1jEXhJX5pWXZhKu68130_provenance.
- NP583192.RA_dLDXxVbpXgIRp21T0rdhvDIjx1jEXhJX5pWXZhKu68130_assertion evidence source_evidence_literature NP583192.RA_dLDXxVbpXgIRp21T0rdhvDIjx1jEXhJX5pWXZhKu68130_provenance.
- NP583192.RA_dLDXxVbpXgIRp21T0rdhvDIjx1jEXhJX5pWXZhKu68130_assertion description "[A myopathy associated with a specific mutation in MYH2 is associated with congenital joint contractures and external ophthalmoplegia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP583192.RA_dLDXxVbpXgIRp21T0rdhvDIjx1jEXhJX5pWXZhKu68130_provenance.