Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP306980.RAfbOQ6WkmglsbI9uieDqbOpOjCsH-c14ZGvrqgEuW210130_assertion> ?p ?o ?g. }
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- NP306980.RAfbOQ6WkmglsbI9uieDqbOpOjCsH-c14ZGvrqgEuW210130_assertion type Assertion NP306980.RAfbOQ6WkmglsbI9uieDqbOpOjCsH-c14ZGvrqgEuW210130_head.
- NP306980.RAfbOQ6WkmglsbI9uieDqbOpOjCsH-c14ZGvrqgEuW210130_assertion wasGeneratedBy ECO_0000203 NP306980.RAfbOQ6WkmglsbI9uieDqbOpOjCsH-c14ZGvrqgEuW210130_provenance.
- NP306980.RAfbOQ6WkmglsbI9uieDqbOpOjCsH-c14ZGvrqgEuW210130_assertion wasDerivedFrom befree-20140225 NP306980.RAfbOQ6WkmglsbI9uieDqbOpOjCsH-c14ZGvrqgEuW210130_provenance.
- NP306980.RAfbOQ6WkmglsbI9uieDqbOpOjCsH-c14ZGvrqgEuW210130_assertion SIO_000772 8058286 NP306980.RAfbOQ6WkmglsbI9uieDqbOpOjCsH-c14ZGvrqgEuW210130_provenance.
- NP306980.RAfbOQ6WkmglsbI9uieDqbOpOjCsH-c14ZGvrqgEuW210130_assertion evidence source_evidence_literature NP306980.RAfbOQ6WkmglsbI9uieDqbOpOjCsH-c14ZGvrqgEuW210130_provenance.
- NP306980.RAfbOQ6WkmglsbI9uieDqbOpOjCsH-c14ZGvrqgEuW210130_assertion description "[Mutations in the human peripherin/retinal degeneration slow (rds) gene have been found in patients with macular dystrophies as well as in those with autosomal dominant retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP306980.RAfbOQ6WkmglsbI9uieDqbOpOjCsH-c14ZGvrqgEuW210130_provenance.