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- NP758326.RA8jJoi-Pu8aTXB2viFbW51lKK5QCgJfKmW7_i30hhatM130_assertion type Assertion NP758326.RA8jJoi-Pu8aTXB2viFbW51lKK5QCgJfKmW7_i30hhatM130_head.
- NP758326.RA8jJoi-Pu8aTXB2viFbW51lKK5QCgJfKmW7_i30hhatM130_assertion wasGeneratedBy ECO_0000203 NP758326.RA8jJoi-Pu8aTXB2viFbW51lKK5QCgJfKmW7_i30hhatM130_provenance.
- NP758326.RA8jJoi-Pu8aTXB2viFbW51lKK5QCgJfKmW7_i30hhatM130_assertion wasDerivedFrom befree-20150227 NP758326.RA8jJoi-Pu8aTXB2viFbW51lKK5QCgJfKmW7_i30hhatM130_provenance.
- NP758326.RA8jJoi-Pu8aTXB2viFbW51lKK5QCgJfKmW7_i30hhatM130_assertion SIO_000772 22971997 NP758326.RA8jJoi-Pu8aTXB2viFbW51lKK5QCgJfKmW7_i30hhatM130_provenance.
- NP758326.RA8jJoi-Pu8aTXB2viFbW51lKK5QCgJfKmW7_i30hhatM130_assertion evidence source_evidence_literature NP758326.RA8jJoi-Pu8aTXB2viFbW51lKK5QCgJfKmW7_i30hhatM130_provenance.
- NP758326.RA8jJoi-Pu8aTXB2viFbW51lKK5QCgJfKmW7_i30hhatM130_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." NP758326.RA8jJoi-Pu8aTXB2viFbW51lKK5QCgJfKmW7_i30hhatM130_provenance.