Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP763059.RAAoqh29fRrnsA8Yqcyg_IOKuy26g7fBNtafy_4wHnM-0130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP763059.RAAoqh29fRrnsA8Yqcyg_IOKuy26g7fBNtafy_4wHnM-0130_assertion type Assertion NP763059.RAAoqh29fRrnsA8Yqcyg_IOKuy26g7fBNtafy_4wHnM-0130_head.
- NP763059.RAAoqh29fRrnsA8Yqcyg_IOKuy26g7fBNtafy_4wHnM-0130_assertion wasGeneratedBy ECO_0000203 NP763059.RAAoqh29fRrnsA8Yqcyg_IOKuy26g7fBNtafy_4wHnM-0130_provenance.
- NP763059.RAAoqh29fRrnsA8Yqcyg_IOKuy26g7fBNtafy_4wHnM-0130_assertion wasDerivedFrom befree-20150227 NP763059.RAAoqh29fRrnsA8Yqcyg_IOKuy26g7fBNtafy_4wHnM-0130_provenance.
- NP763059.RAAoqh29fRrnsA8Yqcyg_IOKuy26g7fBNtafy_4wHnM-0130_assertion SIO_000772 16200211 NP763059.RAAoqh29fRrnsA8Yqcyg_IOKuy26g7fBNtafy_4wHnM-0130_provenance.
- NP763059.RAAoqh29fRrnsA8Yqcyg_IOKuy26g7fBNtafy_4wHnM-0130_assertion evidence source_evidence_literature NP763059.RAAoqh29fRrnsA8Yqcyg_IOKuy26g7fBNtafy_4wHnM-0130_provenance.
- NP763059.RAAoqh29fRrnsA8Yqcyg_IOKuy26g7fBNtafy_4wHnM-0130_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." NP763059.RAAoqh29fRrnsA8Yqcyg_IOKuy26g7fBNtafy_4wHnM-0130_provenance.