Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP854437.RAvrptFXH79QROUK3RfoeC5uvIwdpbdMlpjvA_iMkrh3c130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP854437.RAvrptFXH79QROUK3RfoeC5uvIwdpbdMlpjvA_iMkrh3c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP854437.RAvrptFXH79QROUK3RfoeC5uvIwdpbdMlpjvA_iMkrh3c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP854437.RAvrptFXH79QROUK3RfoeC5uvIwdpbdMlpjvA_iMkrh3c130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP854437.RAvrptFXH79QROUK3RfoeC5uvIwdpbdMlpjvA_iMkrh3c130_provenance.