Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP537772.RAydeq1dvitkZCQ0rvVOdOVUYpYmJsvZFNLuUS4-_2EKQ130_assertion> ?p ?o ?g. }
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- NP537772.RAydeq1dvitkZCQ0rvVOdOVUYpYmJsvZFNLuUS4-_2EKQ130_assertion type Assertion NP537772.RAydeq1dvitkZCQ0rvVOdOVUYpYmJsvZFNLuUS4-_2EKQ130_head.
- NP537772.RAydeq1dvitkZCQ0rvVOdOVUYpYmJsvZFNLuUS4-_2EKQ130_assertion wasGeneratedBy ECO_0000203 NP537772.RAydeq1dvitkZCQ0rvVOdOVUYpYmJsvZFNLuUS4-_2EKQ130_provenance.
- NP537772.RAydeq1dvitkZCQ0rvVOdOVUYpYmJsvZFNLuUS4-_2EKQ130_assertion wasDerivedFrom befree-2016 NP537772.RAydeq1dvitkZCQ0rvVOdOVUYpYmJsvZFNLuUS4-_2EKQ130_provenance.
- NP537772.RAydeq1dvitkZCQ0rvVOdOVUYpYmJsvZFNLuUS4-_2EKQ130_assertion SIO_000772 16505158 NP537772.RAydeq1dvitkZCQ0rvVOdOVUYpYmJsvZFNLuUS4-_2EKQ130_provenance.
- NP537772.RAydeq1dvitkZCQ0rvVOdOVUYpYmJsvZFNLuUS4-_2EKQ130_assertion evidence source_evidence_literature NP537772.RAydeq1dvitkZCQ0rvVOdOVUYpYmJsvZFNLuUS4-_2EKQ130_provenance.
- NP537772.RAydeq1dvitkZCQ0rvVOdOVUYpYmJsvZFNLuUS4-_2EKQ130_assertion description "[CACNA1F mutations cause the retinal disorder, incomplete congenital stationary night blindness (CSNB2), although mutations have also been detected in patients with divergent diagnoses.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP537772.RAydeq1dvitkZCQ0rvVOdOVUYpYmJsvZFNLuUS4-_2EKQ130_provenance.