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- NP220373.RA1KAimQQEmKUZ2trfj--iosNz6grGLcF1x4zbXaRmUuw130_assertion type Assertion NP220373.RA1KAimQQEmKUZ2trfj--iosNz6grGLcF1x4zbXaRmUuw130_head.
- NP220373.RA1KAimQQEmKUZ2trfj--iosNz6grGLcF1x4zbXaRmUuw130_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." NP220373.RA1KAimQQEmKUZ2trfj--iosNz6grGLcF1x4zbXaRmUuw130_provenance.
- NP220373.RA1KAimQQEmKUZ2trfj--iosNz6grGLcF1x4zbXaRmUuw130_assertion evidence source_evidence_literature NP220373.RA1KAimQQEmKUZ2trfj--iosNz6grGLcF1x4zbXaRmUuw130_provenance.
- NP220373.RA1KAimQQEmKUZ2trfj--iosNz6grGLcF1x4zbXaRmUuw130_assertion SIO_000772 11134486 NP220373.RA1KAimQQEmKUZ2trfj--iosNz6grGLcF1x4zbXaRmUuw130_provenance.
- NP220373.RA1KAimQQEmKUZ2trfj--iosNz6grGLcF1x4zbXaRmUuw130_assertion wasDerivedFrom befree-20150227 NP220373.RA1KAimQQEmKUZ2trfj--iosNz6grGLcF1x4zbXaRmUuw130_provenance.
- NP220373.RA1KAimQQEmKUZ2trfj--iosNz6grGLcF1x4zbXaRmUuw130_assertion wasGeneratedBy ECO_0000203 NP220373.RA1KAimQQEmKUZ2trfj--iosNz6grGLcF1x4zbXaRmUuw130_provenance.