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- NP283252.RA_1pPfvuvHPi8561cbDrO30UXD4bAJyDC5ZyluMdG42E130_assertion type Assertion NP283252.RA_1pPfvuvHPi8561cbDrO30UXD4bAJyDC5ZyluMdG42E130_head.
- NP283252.RA_1pPfvuvHPi8561cbDrO30UXD4bAJyDC5ZyluMdG42E130_assertion wasGeneratedBy ECO_0000203 NP283252.RA_1pPfvuvHPi8561cbDrO30UXD4bAJyDC5ZyluMdG42E130_provenance.
- NP283252.RA_1pPfvuvHPi8561cbDrO30UXD4bAJyDC5ZyluMdG42E130_assertion wasDerivedFrom befree-2016 NP283252.RA_1pPfvuvHPi8561cbDrO30UXD4bAJyDC5ZyluMdG42E130_provenance.
- NP283252.RA_1pPfvuvHPi8561cbDrO30UXD4bAJyDC5ZyluMdG42E130_assertion SIO_000772 10802659 NP283252.RA_1pPfvuvHPi8561cbDrO30UXD4bAJyDC5ZyluMdG42E130_provenance.
- NP283252.RA_1pPfvuvHPi8561cbDrO30UXD4bAJyDC5ZyluMdG42E130_assertion evidence source_evidence_literature NP283252.RA_1pPfvuvHPi8561cbDrO30UXD4bAJyDC5ZyluMdG42E130_provenance.
- NP283252.RA_1pPfvuvHPi8561cbDrO30UXD4bAJyDC5ZyluMdG42E130_assertion description "[6), and mutations in RDS (the human homologue of Prph2) cause retinal degeneration, the relationship of Rom-1 to these processes is uncertain.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP283252.RA_1pPfvuvHPi8561cbDrO30UXD4bAJyDC5ZyluMdG42E130_provenance.