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- NP887726.RALx22U_wlSmzz3HWpMaN1cLWchhTS4v3N0Q4aHGLdsYQ130_assertion type Assertion NP887726.RALx22U_wlSmzz3HWpMaN1cLWchhTS4v3N0Q4aHGLdsYQ130_head.
- NP887726.RALx22U_wlSmzz3HWpMaN1cLWchhTS4v3N0Q4aHGLdsYQ130_assertion description "[FHL1 mutations cause Emery-Dreifuss muscular dystrophy (OMIM 310300), X-linked myopathy with postural muscle atrophy (XMPMA, OMIM 300696), scapuloperoneal myopathy (OMIM 300695), or reducing body myopathy (OMIM 300717, 300718).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP887726.RALx22U_wlSmzz3HWpMaN1cLWchhTS4v3N0Q4aHGLdsYQ130_provenance.
- NP887726.RALx22U_wlSmzz3HWpMaN1cLWchhTS4v3N0Q4aHGLdsYQ130_assertion evidence source_evidence_literature NP887726.RALx22U_wlSmzz3HWpMaN1cLWchhTS4v3N0Q4aHGLdsYQ130_provenance.
- NP887726.RALx22U_wlSmzz3HWpMaN1cLWchhTS4v3N0Q4aHGLdsYQ130_assertion SIO_000772 21932316 NP887726.RALx22U_wlSmzz3HWpMaN1cLWchhTS4v3N0Q4aHGLdsYQ130_provenance.
- NP887726.RALx22U_wlSmzz3HWpMaN1cLWchhTS4v3N0Q4aHGLdsYQ130_assertion wasDerivedFrom befree-20150227 NP887726.RALx22U_wlSmzz3HWpMaN1cLWchhTS4v3N0Q4aHGLdsYQ130_provenance.
- NP887726.RALx22U_wlSmzz3HWpMaN1cLWchhTS4v3N0Q4aHGLdsYQ130_assertion wasGeneratedBy ECO_0000203 NP887726.RALx22U_wlSmzz3HWpMaN1cLWchhTS4v3N0Q4aHGLdsYQ130_provenance.