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- NP396738.RADaC3CMqXy01sGRJrtDZ99HibOPAJeTkFixiUP-2ojok130_assertion type Assertion NP396738.RADaC3CMqXy01sGRJrtDZ99HibOPAJeTkFixiUP-2ojok130_head.
- NP396738.RADaC3CMqXy01sGRJrtDZ99HibOPAJeTkFixiUP-2ojok130_assertion wasGeneratedBy ECO_0000203 NP396738.RADaC3CMqXy01sGRJrtDZ99HibOPAJeTkFixiUP-2ojok130_provenance.
- NP396738.RADaC3CMqXy01sGRJrtDZ99HibOPAJeTkFixiUP-2ojok130_assertion wasDerivedFrom befree-2016 NP396738.RADaC3CMqXy01sGRJrtDZ99HibOPAJeTkFixiUP-2ojok130_provenance.
- NP396738.RADaC3CMqXy01sGRJrtDZ99HibOPAJeTkFixiUP-2ojok130_assertion SIO_000772 12783988 NP396738.RADaC3CMqXy01sGRJrtDZ99HibOPAJeTkFixiUP-2ojok130_provenance.
- NP396738.RADaC3CMqXy01sGRJrtDZ99HibOPAJeTkFixiUP-2ojok130_assertion evidence source_evidence_literature NP396738.RADaC3CMqXy01sGRJrtDZ99HibOPAJeTkFixiUP-2ojok130_provenance.
- NP396738.RADaC3CMqXy01sGRJrtDZ99HibOPAJeTkFixiUP-2ojok130_assertion description "[Mutations in lamin A/C can cause Emery-Dreifuss muscular dystrophy (EDMD) or a related cardiomyopathy (CMD1A).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP396738.RADaC3CMqXy01sGRJrtDZ99HibOPAJeTkFixiUP-2ojok130_provenance.