Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP386054.RAzL6ZQa1_9xBYzhv3x0A64jZKReZUxCaqiO5uybVCHaY130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP386054.RAzL6ZQa1_9xBYzhv3x0A64jZKReZUxCaqiO5uybVCHaY130_assertion type Assertion NP386054.RAzL6ZQa1_9xBYzhv3x0A64jZKReZUxCaqiO5uybVCHaY130_head.
- NP386054.RAzL6ZQa1_9xBYzhv3x0A64jZKReZUxCaqiO5uybVCHaY130_assertion description "[The myopathic form of coenzyme Q10 deficiency is caused by mutations in the electron-transferring-flavoprotein dehydrogenase (ETFDH) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP386054.RAzL6ZQa1_9xBYzhv3x0A64jZKReZUxCaqiO5uybVCHaY130_provenance.
- NP386054.RAzL6ZQa1_9xBYzhv3x0A64jZKReZUxCaqiO5uybVCHaY130_assertion evidence source_evidence_literature NP386054.RAzL6ZQa1_9xBYzhv3x0A64jZKReZUxCaqiO5uybVCHaY130_provenance.
- NP386054.RAzL6ZQa1_9xBYzhv3x0A64jZKReZUxCaqiO5uybVCHaY130_assertion SIO_000772 17412732 NP386054.RAzL6ZQa1_9xBYzhv3x0A64jZKReZUxCaqiO5uybVCHaY130_provenance.
- NP386054.RAzL6ZQa1_9xBYzhv3x0A64jZKReZUxCaqiO5uybVCHaY130_assertion wasDerivedFrom befree-20150227 NP386054.RAzL6ZQa1_9xBYzhv3x0A64jZKReZUxCaqiO5uybVCHaY130_provenance.
- NP386054.RAzL6ZQa1_9xBYzhv3x0A64jZKReZUxCaqiO5uybVCHaY130_assertion wasGeneratedBy ECO_0000203 NP386054.RAzL6ZQa1_9xBYzhv3x0A64jZKReZUxCaqiO5uybVCHaY130_provenance.