Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP676401.RA1WvxRR5QN9kUgTgzFOtuylf-omRhBqKbSl7l96YFzSE130_assertion> ?p ?o ?g. }
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- NP676401.RA1WvxRR5QN9kUgTgzFOtuylf-omRhBqKbSl7l96YFzSE130_assertion type Assertion NP676401.RA1WvxRR5QN9kUgTgzFOtuylf-omRhBqKbSl7l96YFzSE130_head.
- NP676401.RA1WvxRR5QN9kUgTgzFOtuylf-omRhBqKbSl7l96YFzSE130_assertion description "[Three of the patients were homozygous for the 'common' 1528G>C mutation in the alpha-subunit of the MTP, giving rise to long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP676401.RA1WvxRR5QN9kUgTgzFOtuylf-omRhBqKbSl7l96YFzSE130_provenance.
- NP676401.RA1WvxRR5QN9kUgTgzFOtuylf-omRhBqKbSl7l96YFzSE130_assertion evidence source_evidence_literature NP676401.RA1WvxRR5QN9kUgTgzFOtuylf-omRhBqKbSl7l96YFzSE130_provenance.
- NP676401.RA1WvxRR5QN9kUgTgzFOtuylf-omRhBqKbSl7l96YFzSE130_assertion SIO_000772 14605499 NP676401.RA1WvxRR5QN9kUgTgzFOtuylf-omRhBqKbSl7l96YFzSE130_provenance.
- NP676401.RA1WvxRR5QN9kUgTgzFOtuylf-omRhBqKbSl7l96YFzSE130_assertion wasDerivedFrom befree-20140225 NP676401.RA1WvxRR5QN9kUgTgzFOtuylf-omRhBqKbSl7l96YFzSE130_provenance.
- NP676401.RA1WvxRR5QN9kUgTgzFOtuylf-omRhBqKbSl7l96YFzSE130_assertion wasGeneratedBy ECO_0000203 NP676401.RA1WvxRR5QN9kUgTgzFOtuylf-omRhBqKbSl7l96YFzSE130_provenance.