Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1316492.RA_fen_YKG1OEI-Z-MbGNxtisdZpAzOKhCmERHLt07o6I130_assertion> ?p ?o ?g. }
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- NP1316492.RA_fen_YKG1OEI-Z-MbGNxtisdZpAzOKhCmERHLt07o6I130_assertion type Assertion NP1316492.RA_fen_YKG1OEI-Z-MbGNxtisdZpAzOKhCmERHLt07o6I130_head.
- NP1316492.RA_fen_YKG1OEI-Z-MbGNxtisdZpAzOKhCmERHLt07o6I130_assertion description "[The mutation in the mitochondrial ATP synthase subunit 6 gene (ATP6 T8993G) was identified in a male infant who died at age 15 months of Leigh syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1316492.RA_fen_YKG1OEI-Z-MbGNxtisdZpAzOKhCmERHLt07o6I130_provenance.
- NP1316492.RA_fen_YKG1OEI-Z-MbGNxtisdZpAzOKhCmERHLt07o6I130_assertion evidence source_evidence_literature NP1316492.RA_fen_YKG1OEI-Z-MbGNxtisdZpAzOKhCmERHLt07o6I130_provenance.
- NP1316492.RA_fen_YKG1OEI-Z-MbGNxtisdZpAzOKhCmERHLt07o6I130_assertion SIO_000772 7649544 NP1316492.RA_fen_YKG1OEI-Z-MbGNxtisdZpAzOKhCmERHLt07o6I130_provenance.
- NP1316492.RA_fen_YKG1OEI-Z-MbGNxtisdZpAzOKhCmERHLt07o6I130_assertion wasDerivedFrom befree-2016 NP1316492.RA_fen_YKG1OEI-Z-MbGNxtisdZpAzOKhCmERHLt07o6I130_provenance.
- NP1316492.RA_fen_YKG1OEI-Z-MbGNxtisdZpAzOKhCmERHLt07o6I130_assertion wasGeneratedBy ECO_0000203 NP1316492.RA_fen_YKG1OEI-Z-MbGNxtisdZpAzOKhCmERHLt07o6I130_provenance.