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- NP668466.RAxxtkeNBvcfYIX2DOJ3jrMjH18Q5HCKi_6qr8ZQzCkpY130_assertion type Assertion NP668466.RAxxtkeNBvcfYIX2DOJ3jrMjH18Q5HCKi_6qr8ZQzCkpY130_head.
- NP668466.RAxxtkeNBvcfYIX2DOJ3jrMjH18Q5HCKi_6qr8ZQzCkpY130_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." NP668466.RAxxtkeNBvcfYIX2DOJ3jrMjH18Q5HCKi_6qr8ZQzCkpY130_provenance.
- NP668466.RAxxtkeNBvcfYIX2DOJ3jrMjH18Q5HCKi_6qr8ZQzCkpY130_assertion evidence source_evidence_literature NP668466.RAxxtkeNBvcfYIX2DOJ3jrMjH18Q5HCKi_6qr8ZQzCkpY130_provenance.
- NP668466.RAxxtkeNBvcfYIX2DOJ3jrMjH18Q5HCKi_6qr8ZQzCkpY130_assertion SIO_000772 10369264 NP668466.RAxxtkeNBvcfYIX2DOJ3jrMjH18Q5HCKi_6qr8ZQzCkpY130_provenance.
- NP668466.RAxxtkeNBvcfYIX2DOJ3jrMjH18Q5HCKi_6qr8ZQzCkpY130_assertion wasDerivedFrom befree-20150227 NP668466.RAxxtkeNBvcfYIX2DOJ3jrMjH18Q5HCKi_6qr8ZQzCkpY130_provenance.
- NP668466.RAxxtkeNBvcfYIX2DOJ3jrMjH18Q5HCKi_6qr8ZQzCkpY130_assertion wasGeneratedBy ECO_0000203 NP668466.RAxxtkeNBvcfYIX2DOJ3jrMjH18Q5HCKi_6qr8ZQzCkpY130_provenance.