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- NP255058.RA6V9fWlt0ghb3lAOEYIkR8ikhe3Y0bjBSNFATNmMgGH0130_assertion type Assertion NP255058.RA6V9fWlt0ghb3lAOEYIkR8ikhe3Y0bjBSNFATNmMgGH0130_head.
- NP255058.RA6V9fWlt0ghb3lAOEYIkR8ikhe3Y0bjBSNFATNmMgGH0130_assertion description "[We evaluated patients with hereditary retinal diseases featuring subretinal spots (retinitis punctata albescens and fundus albipunctatus) and patients with typical dominant or recessive retinitis pigmentosa for mutations in RDH5.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP255058.RA6V9fWlt0ghb3lAOEYIkR8ikhe3Y0bjBSNFATNmMgGH0130_provenance.
- NP255058.RA6V9fWlt0ghb3lAOEYIkR8ikhe3Y0bjBSNFATNmMgGH0130_assertion evidence source_evidence_literature NP255058.RA6V9fWlt0ghb3lAOEYIkR8ikhe3Y0bjBSNFATNmMgGH0130_provenance.
- NP255058.RA6V9fWlt0ghb3lAOEYIkR8ikhe3Y0bjBSNFATNmMgGH0130_assertion SIO_000772 10369264 NP255058.RA6V9fWlt0ghb3lAOEYIkR8ikhe3Y0bjBSNFATNmMgGH0130_provenance.
- NP255058.RA6V9fWlt0ghb3lAOEYIkR8ikhe3Y0bjBSNFATNmMgGH0130_assertion wasDerivedFrom befree-2016 NP255058.RA6V9fWlt0ghb3lAOEYIkR8ikhe3Y0bjBSNFATNmMgGH0130_provenance.
- NP255058.RA6V9fWlt0ghb3lAOEYIkR8ikhe3Y0bjBSNFATNmMgGH0130_assertion wasGeneratedBy ECO_0000203 NP255058.RA6V9fWlt0ghb3lAOEYIkR8ikhe3Y0bjBSNFATNmMgGH0130_provenance.