Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP329587.RAtFzflcW97zLo3OVlWfpKFMM53CXuLKq0koJqJfBBUQ0130_assertion> ?p ?o ?g. }
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- NP329587.RAtFzflcW97zLo3OVlWfpKFMM53CXuLKq0koJqJfBBUQ0130_assertion type Assertion NP329587.RAtFzflcW97zLo3OVlWfpKFMM53CXuLKq0koJqJfBBUQ0130_head.
- NP329587.RAtFzflcW97zLo3OVlWfpKFMM53CXuLKq0koJqJfBBUQ0130_assertion description "[Mutations in ABCA4 have been associated with autosomal recessive Stargardt disease (STGD), a few cases with autosomal recessive cone-rod dystrophy (arCRD) and autosomal recessive retinitis pigmentosa (arRP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP329587.RAtFzflcW97zLo3OVlWfpKFMM53CXuLKq0koJqJfBBUQ0130_provenance.
- NP329587.RAtFzflcW97zLo3OVlWfpKFMM53CXuLKq0koJqJfBBUQ0130_assertion evidence source_evidence_literature NP329587.RAtFzflcW97zLo3OVlWfpKFMM53CXuLKq0koJqJfBBUQ0130_provenance.
- NP329587.RAtFzflcW97zLo3OVlWfpKFMM53CXuLKq0koJqJfBBUQ0130_assertion SIO_000772 19028736 NP329587.RAtFzflcW97zLo3OVlWfpKFMM53CXuLKq0koJqJfBBUQ0130_provenance.
- NP329587.RAtFzflcW97zLo3OVlWfpKFMM53CXuLKq0koJqJfBBUQ0130_assertion wasDerivedFrom befree-20140225 NP329587.RAtFzflcW97zLo3OVlWfpKFMM53CXuLKq0koJqJfBBUQ0130_provenance.
- NP329587.RAtFzflcW97zLo3OVlWfpKFMM53CXuLKq0koJqJfBBUQ0130_assertion wasGeneratedBy ECO_0000203 NP329587.RAtFzflcW97zLo3OVlWfpKFMM53CXuLKq0koJqJfBBUQ0130_provenance.