Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP828633.RA1-d-sEKt1G2bfTokk_-bMBbkkRP5xNz0xTOu0I9n6xs130_assertion> ?p ?o ?g. }
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- NP828633.RA1-d-sEKt1G2bfTokk_-bMBbkkRP5xNz0xTOu0I9n6xs130_assertion type Assertion NP828633.RA1-d-sEKt1G2bfTokk_-bMBbkkRP5xNz0xTOu0I9n6xs130_head.
- NP828633.RA1-d-sEKt1G2bfTokk_-bMBbkkRP5xNz0xTOu0I9n6xs130_assertion description "[Mutations in RLBP1 were identified in 7 patients with RPA and in 1 patient with FAP and cone dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP828633.RA1-d-sEKt1G2bfTokk_-bMBbkkRP5xNz0xTOu0I9n6xs130_provenance.
- NP828633.RA1-d-sEKt1G2bfTokk_-bMBbkkRP5xNz0xTOu0I9n6xs130_assertion evidence source_evidence_literature NP828633.RA1-d-sEKt1G2bfTokk_-bMBbkkRP5xNz0xTOu0I9n6xs130_provenance.
- NP828633.RA1-d-sEKt1G2bfTokk_-bMBbkkRP5xNz0xTOu0I9n6xs130_assertion SIO_000772 22559933 NP828633.RA1-d-sEKt1G2bfTokk_-bMBbkkRP5xNz0xTOu0I9n6xs130_provenance.
- NP828633.RA1-d-sEKt1G2bfTokk_-bMBbkkRP5xNz0xTOu0I9n6xs130_assertion wasDerivedFrom befree-20140225 NP828633.RA1-d-sEKt1G2bfTokk_-bMBbkkRP5xNz0xTOu0I9n6xs130_provenance.
- NP828633.RA1-d-sEKt1G2bfTokk_-bMBbkkRP5xNz0xTOu0I9n6xs130_assertion wasGeneratedBy ECO_0000203 NP828633.RA1-d-sEKt1G2bfTokk_-bMBbkkRP5xNz0xTOu0I9n6xs130_provenance.