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- NP20321.RADRhHkoa6wjor_ZnVLulseVpabhs6Zi4rF-_NsN_7nG0130_assertion type Assertion NP20321.RADRhHkoa6wjor_ZnVLulseVpabhs6Zi4rF-_NsN_7nG0130_head.
- NP20321.RADRhHkoa6wjor_ZnVLulseVpabhs6Zi4rF-_NsN_7nG0130_assertion description "[Mutations in amphiphysin 2 (BIN1) disrupt interaction with dynamin 2 and cause autosomal recessive centronuclear myopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP20321.RADRhHkoa6wjor_ZnVLulseVpabhs6Zi4rF-_NsN_7nG0130_provenance.
- NP20321.RADRhHkoa6wjor_ZnVLulseVpabhs6Zi4rF-_NsN_7nG0130_assertion evidence source_evidence_curated NP20321.RADRhHkoa6wjor_ZnVLulseVpabhs6Zi4rF-_NsN_7nG0130_provenance.
- NP20321.RADRhHkoa6wjor_ZnVLulseVpabhs6Zi4rF-_NsN_7nG0130_assertion SIO_000772 17676042 NP20321.RADRhHkoa6wjor_ZnVLulseVpabhs6Zi4rF-_NsN_7nG0130_provenance.
- NP20321.RADRhHkoa6wjor_ZnVLulseVpabhs6Zi4rF-_NsN_7nG0130_assertion wasDerivedFrom ctd_human-2016 NP20321.RADRhHkoa6wjor_ZnVLulseVpabhs6Zi4rF-_NsN_7nG0130_provenance.
- NP20321.RADRhHkoa6wjor_ZnVLulseVpabhs6Zi4rF-_NsN_7nG0130_assertion wasGeneratedBy ECO_0000218 NP20321.RADRhHkoa6wjor_ZnVLulseVpabhs6Zi4rF-_NsN_7nG0130_provenance.