Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP760947.RAhFpPrg4RllMMfrMv6oGN1hdyByZ0JhiQQF1oUn5Q3i8130_assertion> ?p ?o ?g. }
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- NP760947.RAhFpPrg4RllMMfrMv6oGN1hdyByZ0JhiQQF1oUn5Q3i8130_assertion type Assertion NP760947.RAhFpPrg4RllMMfrMv6oGN1hdyByZ0JhiQQF1oUn5Q3i8130_head.
- NP760947.RAhFpPrg4RllMMfrMv6oGN1hdyByZ0JhiQQF1oUn5Q3i8130_assertion description "[The absence of detectable peripherin/RDS mutations in these families suggests either that: (i) mutations in other digenic partners are required for pathogenic ROM1 alleles to cause retinal degeneration; (ii) these ROM1 mutations do not cause RP; or (iii) peripherin/RDS mutations are present but were not identified in these patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP760947.RAhFpPrg4RllMMfrMv6oGN1hdyByZ0JhiQQF1oUn5Q3i8130_provenance.
- NP760947.RAhFpPrg4RllMMfrMv6oGN1hdyByZ0JhiQQF1oUn5Q3i8130_assertion evidence source_evidence_literature NP760947.RAhFpPrg4RllMMfrMv6oGN1hdyByZ0JhiQQF1oUn5Q3i8130_provenance.
- NP760947.RAhFpPrg4RllMMfrMv6oGN1hdyByZ0JhiQQF1oUn5Q3i8130_assertion SIO_000772 8595413 NP760947.RAhFpPrg4RllMMfrMv6oGN1hdyByZ0JhiQQF1oUn5Q3i8130_provenance.
- NP760947.RAhFpPrg4RllMMfrMv6oGN1hdyByZ0JhiQQF1oUn5Q3i8130_assertion wasDerivedFrom befree-20150227 NP760947.RAhFpPrg4RllMMfrMv6oGN1hdyByZ0JhiQQF1oUn5Q3i8130_provenance.
- NP760947.RAhFpPrg4RllMMfrMv6oGN1hdyByZ0JhiQQF1oUn5Q3i8130_assertion wasGeneratedBy ECO_0000203 NP760947.RAhFpPrg4RllMMfrMv6oGN1hdyByZ0JhiQQF1oUn5Q3i8130_provenance.