Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP310025.RAjM6C0X4yix6Odmam4QbpERhTHwZa7QF5heMOnE3d79k130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP310025.RAjM6C0X4yix6Odmam4QbpERhTHwZa7QF5heMOnE3d79k130_assertion type Assertion NP310025.RAjM6C0X4yix6Odmam4QbpERhTHwZa7QF5heMOnE3d79k130_head.
- NP310025.RAjM6C0X4yix6Odmam4QbpERhTHwZa7QF5heMOnE3d79k130_assertion description "[Persistent trimethylaminuria in children is caused by autosomal recessively inherited impairment of hepatic trimethylamine (TMA) oxidation due to deficiency of flavin monooxygenase 3 (FMO3) secondary to mutations in the FMO3 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP310025.RAjM6C0X4yix6Odmam4QbpERhTHwZa7QF5heMOnE3d79k130_provenance.
- NP310025.RAjM6C0X4yix6Odmam4QbpERhTHwZa7QF5heMOnE3d79k130_assertion evidence source_evidence_literature NP310025.RAjM6C0X4yix6Odmam4QbpERhTHwZa7QF5heMOnE3d79k130_provenance.
- NP310025.RAjM6C0X4yix6Odmam4QbpERhTHwZa7QF5heMOnE3d79k130_assertion SIO_000772 16601883 NP310025.RAjM6C0X4yix6Odmam4QbpERhTHwZa7QF5heMOnE3d79k130_provenance.
- NP310025.RAjM6C0X4yix6Odmam4QbpERhTHwZa7QF5heMOnE3d79k130_assertion wasDerivedFrom befree-20140225 NP310025.RAjM6C0X4yix6Odmam4QbpERhTHwZa7QF5heMOnE3d79k130_provenance.
- NP310025.RAjM6C0X4yix6Odmam4QbpERhTHwZa7QF5heMOnE3d79k130_assertion wasGeneratedBy ECO_0000203 NP310025.RAjM6C0X4yix6Odmam4QbpERhTHwZa7QF5heMOnE3d79k130_provenance.