Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP711091.RAybrk1GA76wbbmENJjVGC0dg07opxozsR7miWRm9L8ds130_assertion> ?p ?o ?g. }
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- NP711091.RAybrk1GA76wbbmENJjVGC0dg07opxozsR7miWRm9L8ds130_assertion type Assertion NP711091.RAybrk1GA76wbbmENJjVGC0dg07opxozsR7miWRm9L8ds130_head.
- NP711091.RAybrk1GA76wbbmENJjVGC0dg07opxozsR7miWRm9L8ds130_assertion description "[One patient was found to have Leigh syndrome due to a mutation in MT-ATP6, two affected siblings were discovered to be compound heterozygous for mutations in the NDUFV1 gene, which causes mitochondrial complex I deficiency, and one patient was found to have coenzyme Q10 deficiency due to compound heterozygous mutations in COQ2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP711091.RAybrk1GA76wbbmENJjVGC0dg07opxozsR7miWRm9L8ds130_provenance.
- NP711091.RAybrk1GA76wbbmENJjVGC0dg07opxozsR7miWRm9L8ds130_assertion evidence source_evidence_literature NP711091.RAybrk1GA76wbbmENJjVGC0dg07opxozsR7miWRm9L8ds130_provenance.
- NP711091.RAybrk1GA76wbbmENJjVGC0dg07opxozsR7miWRm9L8ds130_assertion SIO_000772 23631824 NP711091.RAybrk1GA76wbbmENJjVGC0dg07opxozsR7miWRm9L8ds130_provenance.
- NP711091.RAybrk1GA76wbbmENJjVGC0dg07opxozsR7miWRm9L8ds130_assertion wasDerivedFrom befree-20140225 NP711091.RAybrk1GA76wbbmENJjVGC0dg07opxozsR7miWRm9L8ds130_provenance.
- NP711091.RAybrk1GA76wbbmENJjVGC0dg07opxozsR7miWRm9L8ds130_assertion wasGeneratedBy ECO_0000203 NP711091.RAybrk1GA76wbbmENJjVGC0dg07opxozsR7miWRm9L8ds130_provenance.