Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP809444.RAXBrJ4zQXl9KyDpH-6jUlrP3M9C846XrTm3MdXabMQqA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP809444.RAXBrJ4zQXl9KyDpH-6jUlrP3M9C846XrTm3MdXabMQqA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP809444.RAXBrJ4zQXl9KyDpH-6jUlrP3M9C846XrTm3MdXabMQqA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP809444.RAXBrJ4zQXl9KyDpH-6jUlrP3M9C846XrTm3MdXabMQqA130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP809444.RAXBrJ4zQXl9KyDpH-6jUlrP3M9C846XrTm3MdXabMQqA130_provenance.