Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP800061.RA42Q7VMbBDo8oPt15bZ59PBKHISyNGalf-Sk2e95I7D4130_assertion> ?p ?o ?g. }
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- NP800061.RA42Q7VMbBDo8oPt15bZ59PBKHISyNGalf-Sk2e95I7D4130_assertion type Assertion NP800061.RA42Q7VMbBDo8oPt15bZ59PBKHISyNGalf-Sk2e95I7D4130_head.
- NP800061.RA42Q7VMbBDo8oPt15bZ59PBKHISyNGalf-Sk2e95I7D4130_assertion wasGeneratedBy ECO_0000203 NP800061.RA42Q7VMbBDo8oPt15bZ59PBKHISyNGalf-Sk2e95I7D4130_provenance.
- NP800061.RA42Q7VMbBDo8oPt15bZ59PBKHISyNGalf-Sk2e95I7D4130_assertion wasDerivedFrom befree-20150227 NP800061.RA42Q7VMbBDo8oPt15bZ59PBKHISyNGalf-Sk2e95I7D4130_provenance.
- NP800061.RA42Q7VMbBDo8oPt15bZ59PBKHISyNGalf-Sk2e95I7D4130_assertion SIO_000772 16200211 NP800061.RA42Q7VMbBDo8oPt15bZ59PBKHISyNGalf-Sk2e95I7D4130_provenance.
- NP800061.RA42Q7VMbBDo8oPt15bZ59PBKHISyNGalf-Sk2e95I7D4130_assertion evidence source_evidence_literature NP800061.RA42Q7VMbBDo8oPt15bZ59PBKHISyNGalf-Sk2e95I7D4130_provenance.
- NP800061.RA42Q7VMbBDo8oPt15bZ59PBKHISyNGalf-Sk2e95I7D4130_assertion description "[NADH:ubiquinone oxidoreductase (complex I) deficiency is a common cause of mitochondrial oxidative phosphorylation disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP800061.RA42Q7VMbBDo8oPt15bZ59PBKHISyNGalf-Sk2e95I7D4130_provenance.