Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP854437.RAvrptFXH79QROUK3RfoeC5uvIwdpbdMlpjvA_iMkrh3c130_assertion> ?p ?o ?g. }
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- NP854437.RAvrptFXH79QROUK3RfoeC5uvIwdpbdMlpjvA_iMkrh3c130_assertion type Assertion NP854437.RAvrptFXH79QROUK3RfoeC5uvIwdpbdMlpjvA_iMkrh3c130_head.
- 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.
- NP854437.RAvrptFXH79QROUK3RfoeC5uvIwdpbdMlpjvA_iMkrh3c130_assertion evidence source_evidence_literature NP854437.RAvrptFXH79QROUK3RfoeC5uvIwdpbdMlpjvA_iMkrh3c130_provenance.
- NP854437.RAvrptFXH79QROUK3RfoeC5uvIwdpbdMlpjvA_iMkrh3c130_assertion SIO_000772 17132746 NP854437.RAvrptFXH79QROUK3RfoeC5uvIwdpbdMlpjvA_iMkrh3c130_provenance.
- NP854437.RAvrptFXH79QROUK3RfoeC5uvIwdpbdMlpjvA_iMkrh3c130_assertion wasDerivedFrom befree-20140225 NP854437.RAvrptFXH79QROUK3RfoeC5uvIwdpbdMlpjvA_iMkrh3c130_provenance.
- NP854437.RAvrptFXH79QROUK3RfoeC5uvIwdpbdMlpjvA_iMkrh3c130_assertion wasGeneratedBy ECO_0000203 NP854437.RAvrptFXH79QROUK3RfoeC5uvIwdpbdMlpjvA_iMkrh3c130_provenance.