Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP310025.RAjM6C0X4yix6Odmam4QbpERhTHwZa7QF5heMOnE3d79k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP310025.RAjM6C0X4yix6Odmam4QbpERhTHwZa7QF5heMOnE3d79k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP310025.RAjM6C0X4yix6Odmam4QbpERhTHwZa7QF5heMOnE3d79k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP310025.RAjM6C0X4yix6Odmam4QbpERhTHwZa7QF5heMOnE3d79k130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP310025.RAjM6C0X4yix6Odmam4QbpERhTHwZa7QF5heMOnE3d79k130_provenance.