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- NP1012504.RAeek6-_l9sVOqdVDODEuP-I9x9Tn5zurWdewwMpMsH5w130_assertion type Assertion NP1012504.RAeek6-_l9sVOqdVDODEuP-I9x9Tn5zurWdewwMpMsH5w130_head.
- NP1012504.RAeek6-_l9sVOqdVDODEuP-I9x9Tn5zurWdewwMpMsH5w130_assertion wasGeneratedBy ECO_0000203 NP1012504.RAeek6-_l9sVOqdVDODEuP-I9x9Tn5zurWdewwMpMsH5w130_provenance.
- NP1012504.RAeek6-_l9sVOqdVDODEuP-I9x9Tn5zurWdewwMpMsH5w130_assertion wasDerivedFrom befree-2016 NP1012504.RAeek6-_l9sVOqdVDODEuP-I9x9Tn5zurWdewwMpMsH5w130_provenance.
- NP1012504.RAeek6-_l9sVOqdVDODEuP-I9x9Tn5zurWdewwMpMsH5w130_assertion SIO_000772 22971997 NP1012504.RAeek6-_l9sVOqdVDODEuP-I9x9Tn5zurWdewwMpMsH5w130_provenance.
- NP1012504.RAeek6-_l9sVOqdVDODEuP-I9x9Tn5zurWdewwMpMsH5w130_assertion evidence source_evidence_literature NP1012504.RAeek6-_l9sVOqdVDODEuP-I9x9Tn5zurWdewwMpMsH5w130_provenance.
- NP1012504.RAeek6-_l9sVOqdVDODEuP-I9x9Tn5zurWdewwMpMsH5w130_assertion description "[The autosomal dominant form of FSGS is a heterogenic disease caused by mutations within three known genes: α-actinin 4 (ACTN4), canonical transient receptor potential 6 (TRPC6), and the inverted formin 2 (INF2) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1012504.RAeek6-_l9sVOqdVDODEuP-I9x9Tn5zurWdewwMpMsH5w130_provenance.