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- NP1743.RAZJ2iQE0T19qnF1vY3k2b9vPwI_vzA4aQ4fxDfzVAiyg130_assertion type Assertion NP1743.RAZJ2iQE0T19qnF1vY3k2b9vPwI_vzA4aQ4fxDfzVAiyg130_head.
- NP1743.RAZJ2iQE0T19qnF1vY3k2b9vPwI_vzA4aQ4fxDfzVAiyg130_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." NP1743.RAZJ2iQE0T19qnF1vY3k2b9vPwI_vzA4aQ4fxDfzVAiyg130_provenance.
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- NP1743.RAZJ2iQE0T19qnF1vY3k2b9vPwI_vzA4aQ4fxDfzVAiyg130_assertion SIO_000772 11134486 NP1743.RAZJ2iQE0T19qnF1vY3k2b9vPwI_vzA4aQ4fxDfzVAiyg130_provenance.
- NP1743.RAZJ2iQE0T19qnF1vY3k2b9vPwI_vzA4aQ4fxDfzVAiyg130_assertion wasDerivedFrom uniprot-20150221 NP1743.RAZJ2iQE0T19qnF1vY3k2b9vPwI_vzA4aQ4fxDfzVAiyg130_provenance.
- NP1743.RAZJ2iQE0T19qnF1vY3k2b9vPwI_vzA4aQ4fxDfzVAiyg130_assertion wasGeneratedBy ECO_0000218 NP1743.RAZJ2iQE0T19qnF1vY3k2b9vPwI_vzA4aQ4fxDfzVAiyg130_provenance.