Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP668516.RAxfyLeMAIiccchzgCfhTdRYCGR-vR5X5FcfNpxNLkCi0130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP668516.RAxfyLeMAIiccchzgCfhTdRYCGR-vR5X5FcfNpxNLkCi0130_assertion type Assertion NP668516.RAxfyLeMAIiccchzgCfhTdRYCGR-vR5X5FcfNpxNLkCi0130_head.
- NP668516.RAxfyLeMAIiccchzgCfhTdRYCGR-vR5X5FcfNpxNLkCi0130_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." NP668516.RAxfyLeMAIiccchzgCfhTdRYCGR-vR5X5FcfNpxNLkCi0130_provenance.
- NP668516.RAxfyLeMAIiccchzgCfhTdRYCGR-vR5X5FcfNpxNLkCi0130_assertion evidence source_evidence_literature NP668516.RAxfyLeMAIiccchzgCfhTdRYCGR-vR5X5FcfNpxNLkCi0130_provenance.
- NP668516.RAxfyLeMAIiccchzgCfhTdRYCGR-vR5X5FcfNpxNLkCi0130_assertion SIO_000772 10369264 NP668516.RAxfyLeMAIiccchzgCfhTdRYCGR-vR5X5FcfNpxNLkCi0130_provenance.
- NP668516.RAxfyLeMAIiccchzgCfhTdRYCGR-vR5X5FcfNpxNLkCi0130_assertion wasDerivedFrom befree-20150227 NP668516.RAxfyLeMAIiccchzgCfhTdRYCGR-vR5X5FcfNpxNLkCi0130_provenance.
- NP668516.RAxfyLeMAIiccchzgCfhTdRYCGR-vR5X5FcfNpxNLkCi0130_assertion wasGeneratedBy ECO_0000203 NP668516.RAxfyLeMAIiccchzgCfhTdRYCGR-vR5X5FcfNpxNLkCi0130_provenance.