Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP229197.RAk0S3CdaEl3lSxne9cgQCVT0_jY6riAP_9-68t6RZyiw130_assertion> ?p ?o ?g. }
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- NP229197.RAk0S3CdaEl3lSxne9cgQCVT0_jY6riAP_9-68t6RZyiw130_assertion type Assertion NP229197.RAk0S3CdaEl3lSxne9cgQCVT0_jY6riAP_9-68t6RZyiw130_head.
- NP229197.RAk0S3CdaEl3lSxne9cgQCVT0_jY6riAP_9-68t6RZyiw130_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." NP229197.RAk0S3CdaEl3lSxne9cgQCVT0_jY6riAP_9-68t6RZyiw130_provenance.
- NP229197.RAk0S3CdaEl3lSxne9cgQCVT0_jY6riAP_9-68t6RZyiw130_assertion evidence source_evidence_literature NP229197.RAk0S3CdaEl3lSxne9cgQCVT0_jY6riAP_9-68t6RZyiw130_provenance.
- NP229197.RAk0S3CdaEl3lSxne9cgQCVT0_jY6riAP_9-68t6RZyiw130_assertion SIO_000772 11134486 NP229197.RAk0S3CdaEl3lSxne9cgQCVT0_jY6riAP_9-68t6RZyiw130_provenance.
- NP229197.RAk0S3CdaEl3lSxne9cgQCVT0_jY6riAP_9-68t6RZyiw130_assertion wasDerivedFrom befree-20140225 NP229197.RAk0S3CdaEl3lSxne9cgQCVT0_jY6riAP_9-68t6RZyiw130_provenance.
- NP229197.RAk0S3CdaEl3lSxne9cgQCVT0_jY6riAP_9-68t6RZyiw130_assertion wasGeneratedBy ECO_0000203 NP229197.RAk0S3CdaEl3lSxne9cgQCVT0_jY6riAP_9-68t6RZyiw130_provenance.