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- NP436159.RA_FsKhezn3P_lafFd5iuNyYer4k6fgU1N4d25Al82lgI130_assertion type Assertion NP436159.RA_FsKhezn3P_lafFd5iuNyYer4k6fgU1N4d25Al82lgI130_head.
- NP436159.RA_FsKhezn3P_lafFd5iuNyYer4k6fgU1N4d25Al82lgI130_assertion description "[Two distinct mutations, a 5-bp deletion and a complex mutation from the same region in exon 6 of this gene, have been reported so far and are associated with autosomal dominant atrophic macular degeneration (adMD/STGD3).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP436159.RA_FsKhezn3P_lafFd5iuNyYer4k6fgU1N4d25Al82lgI130_provenance.
- NP436159.RA_FsKhezn3P_lafFd5iuNyYer4k6fgU1N4d25Al82lgI130_assertion evidence source_evidence_literature NP436159.RA_FsKhezn3P_lafFd5iuNyYer4k6fgU1N4d25Al82lgI130_provenance.
- NP436159.RA_FsKhezn3P_lafFd5iuNyYer4k6fgU1N4d25Al82lgI130_assertion SIO_000772 15028284 NP436159.RA_FsKhezn3P_lafFd5iuNyYer4k6fgU1N4d25Al82lgI130_provenance.
- NP436159.RA_FsKhezn3P_lafFd5iuNyYer4k6fgU1N4d25Al82lgI130_assertion wasDerivedFrom befree-2016 NP436159.RA_FsKhezn3P_lafFd5iuNyYer4k6fgU1N4d25Al82lgI130_provenance.
- NP436159.RA_FsKhezn3P_lafFd5iuNyYer4k6fgU1N4d25Al82lgI130_assertion wasGeneratedBy ECO_0000203 NP436159.RA_FsKhezn3P_lafFd5iuNyYer4k6fgU1N4d25Al82lgI130_provenance.