Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP485609.RAdMyqv7v1lHqveRoobTktxtOBDMiHn_KhI2gPYS_I1IA130_assertion> ?p ?o ?g. }
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- NP485609.RAdMyqv7v1lHqveRoobTktxtOBDMiHn_KhI2gPYS_I1IA130_assertion type Assertion NP485609.RAdMyqv7v1lHqveRoobTktxtOBDMiHn_KhI2gPYS_I1IA130_head.
- NP485609.RAdMyqv7v1lHqveRoobTktxtOBDMiHn_KhI2gPYS_I1IA130_assertion wasGeneratedBy ECO_0000203 NP485609.RAdMyqv7v1lHqveRoobTktxtOBDMiHn_KhI2gPYS_I1IA130_provenance.
- NP485609.RAdMyqv7v1lHqveRoobTktxtOBDMiHn_KhI2gPYS_I1IA130_assertion wasDerivedFrom befree-20140225 NP485609.RAdMyqv7v1lHqveRoobTktxtOBDMiHn_KhI2gPYS_I1IA130_provenance.
- NP485609.RAdMyqv7v1lHqveRoobTktxtOBDMiHn_KhI2gPYS_I1IA130_assertion SIO_000772 8058286 NP485609.RAdMyqv7v1lHqveRoobTktxtOBDMiHn_KhI2gPYS_I1IA130_provenance.
- NP485609.RAdMyqv7v1lHqveRoobTktxtOBDMiHn_KhI2gPYS_I1IA130_assertion evidence source_evidence_literature NP485609.RAdMyqv7v1lHqveRoobTktxtOBDMiHn_KhI2gPYS_I1IA130_provenance.
- NP485609.RAdMyqv7v1lHqveRoobTktxtOBDMiHn_KhI2gPYS_I1IA130_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." NP485609.RAdMyqv7v1lHqveRoobTktxtOBDMiHn_KhI2gPYS_I1IA130_provenance.