Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP463021.RArcu2DByz_1-iQY_Upk_Ku5vBhiykN3ZI7zQ1gb_Mgmg130_assertion> ?p ?o ?g. }
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- NP463021.RArcu2DByz_1-iQY_Upk_Ku5vBhiykN3ZI7zQ1gb_Mgmg130_assertion type Assertion NP463021.RArcu2DByz_1-iQY_Upk_Ku5vBhiykN3ZI7zQ1gb_Mgmg130_head.
- NP463021.RArcu2DByz_1-iQY_Upk_Ku5vBhiykN3ZI7zQ1gb_Mgmg130_assertion description "[Deficiencies in fatty acid metabolism have been extensively studied in cases of SIDS, and by far the most well-investigated mutation is the A985G mutation in the medium-chain acyl-CoA dehydrogenase (MCAD) gene, which is the most prevalent mutation causing MCAD deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP463021.RArcu2DByz_1-iQY_Upk_Ku5vBhiykN3ZI7zQ1gb_Mgmg130_provenance.
- NP463021.RArcu2DByz_1-iQY_Upk_Ku5vBhiykN3ZI7zQ1gb_Mgmg130_assertion evidence source_evidence_literature NP463021.RArcu2DByz_1-iQY_Upk_Ku5vBhiykN3ZI7zQ1gb_Mgmg130_provenance.
- NP463021.RArcu2DByz_1-iQY_Upk_Ku5vBhiykN3ZI7zQ1gb_Mgmg130_assertion SIO_000772 15466077 NP463021.RArcu2DByz_1-iQY_Upk_Ku5vBhiykN3ZI7zQ1gb_Mgmg130_provenance.
- NP463021.RArcu2DByz_1-iQY_Upk_Ku5vBhiykN3ZI7zQ1gb_Mgmg130_assertion wasDerivedFrom befree-2016 NP463021.RArcu2DByz_1-iQY_Upk_Ku5vBhiykN3ZI7zQ1gb_Mgmg130_provenance.
- NP463021.RArcu2DByz_1-iQY_Upk_Ku5vBhiykN3ZI7zQ1gb_Mgmg130_assertion wasGeneratedBy ECO_0000203 NP463021.RArcu2DByz_1-iQY_Upk_Ku5vBhiykN3ZI7zQ1gb_Mgmg130_provenance.