Matches in Nanopublications for { ?s ?p "[Mutations in thiamine transporter gene, SLC19A2, causes a rare form of monogenic diabetes, anemia, and sensorineural deafness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP854437.RAvrptFXH79QROUK3RfoeC5uvIwdpbdMlpjvA_iMkrh3c130_assertion description "[Mutations in thiamine transporter gene, SLC19A2, causes a rare form of monogenic diabetes, anemia, and sensorineural deafness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP854437.RAvrptFXH79QROUK3RfoeC5uvIwdpbdMlpjvA_iMkrh3c130_provenance.