Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP768616.RAnGzcy8-C9mwPoJW2HbUPec_mTMgGg8_ZB-dXCdUXLL0130_assertion> ?p ?o ?g. }
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- NP768616.RAnGzcy8-C9mwPoJW2HbUPec_mTMgGg8_ZB-dXCdUXLL0130_assertion type Assertion NP768616.RAnGzcy8-C9mwPoJW2HbUPec_mTMgGg8_ZB-dXCdUXLL0130_head.
- NP768616.RAnGzcy8-C9mwPoJW2HbUPec_mTMgGg8_ZB-dXCdUXLL0130_assertion description "[Patients with either RGS9/R9AP mutations (bradyopsia) or oligocone trichromacy have very similar clinical phenotypes, characterized by stationary cone dysfunction, mild photophobia, normal color vision, lack of nystagmus, and normal fundi.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP768616.RAnGzcy8-C9mwPoJW2HbUPec_mTMgGg8_ZB-dXCdUXLL0130_provenance.
- NP768616.RAnGzcy8-C9mwPoJW2HbUPec_mTMgGg8_ZB-dXCdUXLL0130_assertion evidence source_evidence_literature NP768616.RAnGzcy8-C9mwPoJW2HbUPec_mTMgGg8_ZB-dXCdUXLL0130_provenance.
- NP768616.RAnGzcy8-C9mwPoJW2HbUPec_mTMgGg8_ZB-dXCdUXLL0130_assertion SIO_000772 19818506 NP768616.RAnGzcy8-C9mwPoJW2HbUPec_mTMgGg8_ZB-dXCdUXLL0130_provenance.
- NP768616.RAnGzcy8-C9mwPoJW2HbUPec_mTMgGg8_ZB-dXCdUXLL0130_assertion wasDerivedFrom befree-2016 NP768616.RAnGzcy8-C9mwPoJW2HbUPec_mTMgGg8_ZB-dXCdUXLL0130_provenance.
- NP768616.RAnGzcy8-C9mwPoJW2HbUPec_mTMgGg8_ZB-dXCdUXLL0130_assertion wasGeneratedBy ECO_0000203 NP768616.RAnGzcy8-C9mwPoJW2HbUPec_mTMgGg8_ZB-dXCdUXLL0130_provenance.