Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP304113.RAF7uGzquW7qLHwpF1-4X8G-peI8BguQ6gOdD1s1RPy6w130_assertion> ?p ?o ?g. }
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- NP304113.RAF7uGzquW7qLHwpF1-4X8G-peI8BguQ6gOdD1s1RPy6w130_assertion type Assertion NP304113.RAF7uGzquW7qLHwpF1-4X8G-peI8BguQ6gOdD1s1RPy6w130_head.
- NP304113.RAF7uGzquW7qLHwpF1-4X8G-peI8BguQ6gOdD1s1RPy6w130_assertion description "[Our findings document that patients carrying these SCAD gene variations may develop clinically relevant SCAD deficiency, and that patients with even mild ethylmalonic aciduria should be tested for these variations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP304113.RAF7uGzquW7qLHwpF1-4X8G-peI8BguQ6gOdD1s1RPy6w130_provenance.
- NP304113.RAF7uGzquW7qLHwpF1-4X8G-peI8BguQ6gOdD1s1RPy6w130_assertion evidence source_evidence_literature NP304113.RAF7uGzquW7qLHwpF1-4X8G-peI8BguQ6gOdD1s1RPy6w130_provenance.
- NP304113.RAF7uGzquW7qLHwpF1-4X8G-peI8BguQ6gOdD1s1RPy6w130_assertion SIO_000772 11134486 NP304113.RAF7uGzquW7qLHwpF1-4X8G-peI8BguQ6gOdD1s1RPy6w130_provenance.
- NP304113.RAF7uGzquW7qLHwpF1-4X8G-peI8BguQ6gOdD1s1RPy6w130_assertion wasDerivedFrom befree-2016 NP304113.RAF7uGzquW7qLHwpF1-4X8G-peI8BguQ6gOdD1s1RPy6w130_provenance.
- NP304113.RAF7uGzquW7qLHwpF1-4X8G-peI8BguQ6gOdD1s1RPy6w130_assertion wasGeneratedBy ECO_0000203 NP304113.RAF7uGzquW7qLHwpF1-4X8G-peI8BguQ6gOdD1s1RPy6w130_provenance.