Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP528882.RA8B-EBL82nkNqIi8Kj4mCtjSIU_CGaZ5-jPWSR0q6Jvc130_assertion> ?p ?o ?g. }
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- NP528882.RA8B-EBL82nkNqIi8Kj4mCtjSIU_CGaZ5-jPWSR0q6Jvc130_assertion type Assertion NP528882.RA8B-EBL82nkNqIi8Kj4mCtjSIU_CGaZ5-jPWSR0q6Jvc130_head.
- NP528882.RA8B-EBL82nkNqIi8Kj4mCtjSIU_CGaZ5-jPWSR0q6Jvc130_assertion wasGeneratedBy ECO_0000203 NP528882.RA8B-EBL82nkNqIi8Kj4mCtjSIU_CGaZ5-jPWSR0q6Jvc130_provenance.
- NP528882.RA8B-EBL82nkNqIi8Kj4mCtjSIU_CGaZ5-jPWSR0q6Jvc130_assertion wasDerivedFrom befree-2016 NP528882.RA8B-EBL82nkNqIi8Kj4mCtjSIU_CGaZ5-jPWSR0q6Jvc130_provenance.
- NP528882.RA8B-EBL82nkNqIi8Kj4mCtjSIU_CGaZ5-jPWSR0q6Jvc130_assertion SIO_000772 16384941 NP528882.RA8B-EBL82nkNqIi8Kj4mCtjSIU_CGaZ5-jPWSR0q6Jvc130_provenance.
- NP528882.RA8B-EBL82nkNqIi8Kj4mCtjSIU_CGaZ5-jPWSR0q6Jvc130_assertion evidence source_evidence_literature NP528882.RA8B-EBL82nkNqIi8Kj4mCtjSIU_CGaZ5-jPWSR0q6Jvc130_provenance.
- NP528882.RA8B-EBL82nkNqIi8Kj4mCtjSIU_CGaZ5-jPWSR0q6Jvc130_assertion description "[Spectrum and frequency of mutations in IMPDH1 associated with autosomal dominant retinitis pigmentosa and leber congenital amaurosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP528882.RA8B-EBL82nkNqIi8Kj4mCtjSIU_CGaZ5-jPWSR0q6Jvc130_provenance.