Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP406133.RACuyqCMlyVcxY1LOpoAQs58vD-M6rPKjif61wFYWvxCE130_assertion> ?p ?o ?g. }
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- NP406133.RACuyqCMlyVcxY1LOpoAQs58vD-M6rPKjif61wFYWvxCE130_assertion type Assertion NP406133.RACuyqCMlyVcxY1LOpoAQs58vD-M6rPKjif61wFYWvxCE130_head.
- NP406133.RACuyqCMlyVcxY1LOpoAQs58vD-M6rPKjif61wFYWvxCE130_assertion description "[Two of the most common clinical presentations, Leigh Syndrome and hypertrophic cardiomyopathy, have so far only been associated with mutations in SURF1 or SCO2 and COX15, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP406133.RACuyqCMlyVcxY1LOpoAQs58vD-M6rPKjif61wFYWvxCE130_provenance.
- NP406133.RACuyqCMlyVcxY1LOpoAQs58vD-M6rPKjif61wFYWvxCE130_assertion evidence source_evidence_literature NP406133.RACuyqCMlyVcxY1LOpoAQs58vD-M6rPKjif61wFYWvxCE130_provenance.
- NP406133.RACuyqCMlyVcxY1LOpoAQs58vD-M6rPKjif61wFYWvxCE130_assertion SIO_000772 12928484 NP406133.RACuyqCMlyVcxY1LOpoAQs58vD-M6rPKjif61wFYWvxCE130_provenance.
- NP406133.RACuyqCMlyVcxY1LOpoAQs58vD-M6rPKjif61wFYWvxCE130_assertion wasDerivedFrom befree-2016 NP406133.RACuyqCMlyVcxY1LOpoAQs58vD-M6rPKjif61wFYWvxCE130_provenance.
- NP406133.RACuyqCMlyVcxY1LOpoAQs58vD-M6rPKjif61wFYWvxCE130_assertion wasGeneratedBy ECO_0000203 NP406133.RACuyqCMlyVcxY1LOpoAQs58vD-M6rPKjif61wFYWvxCE130_provenance.