Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP516030.RA1Xu3HHgQ2EJ27YUmHXb-ZMV0PpK9hlYFJp053dc-fYM130_assertion> ?p ?o ?g. }
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- NP516030.RA1Xu3HHgQ2EJ27YUmHXb-ZMV0PpK9hlYFJp053dc-fYM130_assertion type Assertion NP516030.RA1Xu3HHgQ2EJ27YUmHXb-ZMV0PpK9hlYFJp053dc-fYM130_head.
- NP516030.RA1Xu3HHgQ2EJ27YUmHXb-ZMV0PpK9hlYFJp053dc-fYM130_assertion description "[We found a null mutation in B17.2L in a patient with a progressive encephalopathy and showed that the associated complex I assembly defect could be completely rescued by retroviral expression of B17.2L in patient fibroblasts.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP516030.RA1Xu3HHgQ2EJ27YUmHXb-ZMV0PpK9hlYFJp053dc-fYM130_provenance.
- NP516030.RA1Xu3HHgQ2EJ27YUmHXb-ZMV0PpK9hlYFJp053dc-fYM130_assertion evidence source_evidence_literature NP516030.RA1Xu3HHgQ2EJ27YUmHXb-ZMV0PpK9hlYFJp053dc-fYM130_provenance.
- NP516030.RA1Xu3HHgQ2EJ27YUmHXb-ZMV0PpK9hlYFJp053dc-fYM130_assertion SIO_000772 16200211 NP516030.RA1Xu3HHgQ2EJ27YUmHXb-ZMV0PpK9hlYFJp053dc-fYM130_provenance.
- NP516030.RA1Xu3HHgQ2EJ27YUmHXb-ZMV0PpK9hlYFJp053dc-fYM130_assertion wasDerivedFrom befree-2016 NP516030.RA1Xu3HHgQ2EJ27YUmHXb-ZMV0PpK9hlYFJp053dc-fYM130_provenance.
- NP516030.RA1Xu3HHgQ2EJ27YUmHXb-ZMV0PpK9hlYFJp053dc-fYM130_assertion wasGeneratedBy ECO_0000203 NP516030.RA1Xu3HHgQ2EJ27YUmHXb-ZMV0PpK9hlYFJp053dc-fYM130_provenance.