Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP582379.RACbzsGCI41PyvGlgg8Gn3P8W_2ftli4dUCtc_-UkEcL0130_assertion> ?p ?o ?g. }
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- NP582379.RACbzsGCI41PyvGlgg8Gn3P8W_2ftli4dUCtc_-UkEcL0130_assertion type Assertion NP582379.RACbzsGCI41PyvGlgg8Gn3P8W_2ftli4dUCtc_-UkEcL0130_head.
- NP582379.RACbzsGCI41PyvGlgg8Gn3P8W_2ftli4dUCtc_-UkEcL0130_assertion description "[The patient suffered a sequential optic neuropathy with the hallmarks of LHON and tested positive for the homoplasmic 11778G--> A/ND4 mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP582379.RACbzsGCI41PyvGlgg8Gn3P8W_2ftli4dUCtc_-UkEcL0130_provenance.
- NP582379.RACbzsGCI41PyvGlgg8Gn3P8W_2ftli4dUCtc_-UkEcL0130_assertion evidence source_evidence_literature NP582379.RACbzsGCI41PyvGlgg8Gn3P8W_2ftli4dUCtc_-UkEcL0130_provenance.
- NP582379.RACbzsGCI41PyvGlgg8Gn3P8W_2ftli4dUCtc_-UkEcL0130_assertion SIO_000772 17366829 NP582379.RACbzsGCI41PyvGlgg8Gn3P8W_2ftli4dUCtc_-UkEcL0130_provenance.
- NP582379.RACbzsGCI41PyvGlgg8Gn3P8W_2ftli4dUCtc_-UkEcL0130_assertion wasDerivedFrom befree-20140225 NP582379.RACbzsGCI41PyvGlgg8Gn3P8W_2ftli4dUCtc_-UkEcL0130_provenance.
- NP582379.RACbzsGCI41PyvGlgg8Gn3P8W_2ftli4dUCtc_-UkEcL0130_assertion wasGeneratedBy ECO_0000203 NP582379.RACbzsGCI41PyvGlgg8Gn3P8W_2ftli4dUCtc_-UkEcL0130_provenance.