Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP329587.RAtFzflcW97zLo3OVlWfpKFMM53CXuLKq0koJqJfBBUQ0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP329587.RAtFzflcW97zLo3OVlWfpKFMM53CXuLKq0koJqJfBBUQ0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP329587.RAtFzflcW97zLo3OVlWfpKFMM53CXuLKq0koJqJfBBUQ0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP329587.RAtFzflcW97zLo3OVlWfpKFMM53CXuLKq0koJqJfBBUQ0130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP329587.RAtFzflcW97zLo3OVlWfpKFMM53CXuLKq0koJqJfBBUQ0130_provenance.