Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP66329.RAYZBM-J845p26L8Zrz72-MDgxDBCmJDZg9gQZyOJi2vQ130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP66329.RAYZBM-J845p26L8Zrz72-MDgxDBCmJDZg9gQZyOJi2vQ130_assertion type Assertion NP66329.RAYZBM-J845p26L8Zrz72-MDgxDBCmJDZg9gQZyOJi2vQ130_head.
- NP66329.RAYZBM-J845p26L8Zrz72-MDgxDBCmJDZg9gQZyOJi2vQ130_assertion description "[Mutations in PRPF31, RHO, and PRPH2 were found in low frequencies (1 of 9 autosomal dominant RP families) in Chinese patients, and the PRPF31 and PRPH2 truncating mutations were novel.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66329.RAYZBM-J845p26L8Zrz72-MDgxDBCmJDZg9gQZyOJi2vQ130_provenance.
- NP66329.RAYZBM-J845p26L8Zrz72-MDgxDBCmJDZg9gQZyOJi2vQ130_assertion evidence source_evidence_literature NP66329.RAYZBM-J845p26L8Zrz72-MDgxDBCmJDZg9gQZyOJi2vQ130_provenance.
- NP66329.RAYZBM-J845p26L8Zrz72-MDgxDBCmJDZg9gQZyOJi2vQ130_assertion SIO_000772 19506198 NP66329.RAYZBM-J845p26L8Zrz72-MDgxDBCmJDZg9gQZyOJi2vQ130_provenance.
- NP66329.RAYZBM-J845p26L8Zrz72-MDgxDBCmJDZg9gQZyOJi2vQ130_assertion wasDerivedFrom gad-20130706 NP66329.RAYZBM-J845p26L8Zrz72-MDgxDBCmJDZg9gQZyOJi2vQ130_provenance.
- NP66329.RAYZBM-J845p26L8Zrz72-MDgxDBCmJDZg9gQZyOJi2vQ130_assertion wasGeneratedBy ECO_0000203 NP66329.RAYZBM-J845p26L8Zrz72-MDgxDBCmJDZg9gQZyOJi2vQ130_provenance.