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- NP283999.RA-y60Oa3ft8nnq0alfRQpGkXGq5JjRC--h2LLX6LOkxQ130_assertion type Assertion NP283999.RA-y60Oa3ft8nnq0alfRQpGkXGq5JjRC--h2LLX6LOkxQ130_head.
- NP283999.RA-y60Oa3ft8nnq0alfRQpGkXGq5JjRC--h2LLX6LOkxQ130_assertion wasGeneratedBy ECO_0000203 NP283999.RA-y60Oa3ft8nnq0alfRQpGkXGq5JjRC--h2LLX6LOkxQ130_provenance.
- NP283999.RA-y60Oa3ft8nnq0alfRQpGkXGq5JjRC--h2LLX6LOkxQ130_assertion wasDerivedFrom befree-20140225 NP283999.RA-y60Oa3ft8nnq0alfRQpGkXGq5JjRC--h2LLX6LOkxQ130_provenance.
- NP283999.RA-y60Oa3ft8nnq0alfRQpGkXGq5JjRC--h2LLX6LOkxQ130_assertion SIO_000772 8045710 NP283999.RA-y60Oa3ft8nnq0alfRQpGkXGq5JjRC--h2LLX6LOkxQ130_provenance.
- NP283999.RA-y60Oa3ft8nnq0alfRQpGkXGq5JjRC--h2LLX6LOkxQ130_assertion evidence source_evidence_literature NP283999.RA-y60Oa3ft8nnq0alfRQpGkXGq5JjRC--h2LLX6LOkxQ130_provenance.
- NP283999.RA-y60Oa3ft8nnq0alfRQpGkXGq5JjRC--h2LLX6LOkxQ130_assertion description "[To investigate functional abnormalities in mutations in the peripherin (RDS) gene leading to different clinical types of autosomal dominant retinal disease--macular degeneration and retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP283999.RA-y60Oa3ft8nnq0alfRQpGkXGq5JjRC--h2LLX6LOkxQ130_provenance.