Matches in Nanopublications for { ?s ?p "[Lecithin:cholesterol acyltransferase deficiency: identification of a causative gene mutation and a co-inherited protein polymorphism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP3741.RAdiPQ9xiQ_qkpfnvPy8tCcvw0fS9Llyxk-XSVnoWXjC4130_assertion description "[Lecithin:cholesterol acyltransferase deficiency: identification of a causative gene mutation and a co-inherited protein polymorphism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3741.RAdiPQ9xiQ_qkpfnvPy8tCcvw0fS9Llyxk-XSVnoWXjC4130_provenance.