Matches in Nanopublications for { ?s ?p "[Numerous non-synonymous mutations in FMO3 have been identified in patients suffering from this metabolic disorder (e.g., N61S, M66I, P153L, and R492W), but the molecular mechanism(s) underlying the functional deficit attributed to these alleles has not been elucidated.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP809444.RAXBrJ4zQXl9KyDpH-6jUlrP3M9C846XrTm3MdXabMQqA130_assertion description "[Numerous non-synonymous mutations in FMO3 have been identified in patients suffering from this metabolic disorder (e.g., N61S, M66I, P153L, and R492W), but the molecular mechanism(s) underlying the functional deficit attributed to these alleles has not been elucidated.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP809444.RAXBrJ4zQXl9KyDpH-6jUlrP3M9C846XrTm3MdXabMQqA130_provenance.
- assertion description "[Numerous non-synonymous mutations in FMO3 have been identified in patients suffering from this metabolic disorder (e.g., N61S, M66I, P153L, and R492W), but the molecular mechanism(s) underlying the functional deficit attributed to these alleles has not been elucidated.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP408589.RAhRhJXLEwkjZK-2mWYECOcVE6tSDT1czPJu1JTCwB4Vc130_assertion description "[Numerous non-synonymous mutations in FMO3 have been identified in patients suffering from this metabolic disorder (e.g., N61S, M66I, P153L, and R492W), but the molecular mechanism(s) underlying the functional deficit attributed to these alleles has not been elucidated.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP408589.RAhRhJXLEwkjZK-2mWYECOcVE6tSDT1czPJu1JTCwB4Vc130_provenance.
- NP612125.RAoiTRs3SA7ouKQ0xrQTq0vO5xbXxPW_i1CY7YE4_HJ0c130_assertion description "[Numerous non-synonymous mutations in FMO3 have been identified in patients suffering from this metabolic disorder (e.g., N61S, M66I, P153L, and R492W), but the molecular mechanism(s) underlying the functional deficit attributed to these alleles has not been elucidated.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP612125.RAoiTRs3SA7ouKQ0xrQTq0vO5xbXxPW_i1CY7YE4_HJ0c130_provenance.