Imported Disease Annotations - CTDTerm | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | nephrotic syndrome type 2 | | ISO | NUP205 (Homo sapiens) | 9068941 | CTD Direct Evidence: marker/mechanism | CTD | PMID:26878725 | Paget's disease of bone | | ISO | NUP205 (Homo sapiens) | 9068941 | CTD Direct Evidence: marker/mechanism | CTD | PMID:21623375 | | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Imported Disease Annotations - OMIM
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