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- NP205778.RAN_YnpXpUzD88mWhu0QaD9zBgFYVjOFW7VvPyF04V71A130_assertion type Assertion NP205778.RAN_YnpXpUzD88mWhu0QaD9zBgFYVjOFW7VvPyF04V71A130_head.
- NP205778.RAN_YnpXpUzD88mWhu0QaD9zBgFYVjOFW7VvPyF04V71A130_assertion wasGeneratedBy ECO_0000203 NP205778.RAN_YnpXpUzD88mWhu0QaD9zBgFYVjOFW7VvPyF04V71A130_provenance.
- NP205778.RAN_YnpXpUzD88mWhu0QaD9zBgFYVjOFW7VvPyF04V71A130_assertion wasDerivedFrom lhgdn-20090331 NP205778.RAN_YnpXpUzD88mWhu0QaD9zBgFYVjOFW7VvPyF04V71A130_provenance.
- NP205778.RAN_YnpXpUzD88mWhu0QaD9zBgFYVjOFW7VvPyF04V71A130_assertion SIO_000772 15235026 NP205778.RAN_YnpXpUzD88mWhu0QaD9zBgFYVjOFW7VvPyF04V71A130_provenance.
- NP205778.RAN_YnpXpUzD88mWhu0QaD9zBgFYVjOFW7VvPyF04V71A130_assertion evidence source_evidence_literature NP205778.RAN_YnpXpUzD88mWhu0QaD9zBgFYVjOFW7VvPyF04V71A130_provenance.
- NP205778.RAN_YnpXpUzD88mWhu0QaD9zBgFYVjOFW7VvPyF04V71A130_assertion description "[A patient with typical clinical and neuroradiological features of Leigh syndrome and cytochrome oxidase deficiency was found to have a mutation in the COX15 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205778.RAN_YnpXpUzD88mWhu0QaD9zBgFYVjOFW7VvPyF04V71A130_provenance.