Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP809444.RAXBrJ4zQXl9KyDpH-6jUlrP3M9C846XrTm3MdXabMQqA130_assertion> ?p ?o ?g. }
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- NP809444.RAXBrJ4zQXl9KyDpH-6jUlrP3M9C846XrTm3MdXabMQqA130_assertion type Assertion NP809444.RAXBrJ4zQXl9KyDpH-6jUlrP3M9C846XrTm3MdXabMQqA130_head.
- 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.
- NP809444.RAXBrJ4zQXl9KyDpH-6jUlrP3M9C846XrTm3MdXabMQqA130_assertion evidence source_evidence_literature NP809444.RAXBrJ4zQXl9KyDpH-6jUlrP3M9C846XrTm3MdXabMQqA130_provenance.
- NP809444.RAXBrJ4zQXl9KyDpH-6jUlrP3M9C846XrTm3MdXabMQqA130_assertion SIO_000772 17531949 NP809444.RAXBrJ4zQXl9KyDpH-6jUlrP3M9C846XrTm3MdXabMQqA130_provenance.
- NP809444.RAXBrJ4zQXl9KyDpH-6jUlrP3M9C846XrTm3MdXabMQqA130_assertion wasDerivedFrom befree-20140225 NP809444.RAXBrJ4zQXl9KyDpH-6jUlrP3M9C846XrTm3MdXabMQqA130_provenance.
- NP809444.RAXBrJ4zQXl9KyDpH-6jUlrP3M9C846XrTm3MdXabMQqA130_assertion wasGeneratedBy ECO_0000203 NP809444.RAXBrJ4zQXl9KyDpH-6jUlrP3M9C846XrTm3MdXabMQqA130_provenance.