Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP316740.RArZUQgPPJhYz8dgqxLi1Z5Qz2b0OdhkLCzUP62Vb0N74130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP316740.RArZUQgPPJhYz8dgqxLi1Z5Qz2b0OdhkLCzUP62Vb0N74130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP316740.RArZUQgPPJhYz8dgqxLi1Z5Qz2b0OdhkLCzUP62Vb0N74130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP316740.RArZUQgPPJhYz8dgqxLi1Z5Qz2b0OdhkLCzUP62Vb0N74130_provenance.
- NP316740.RArZUQgPPJhYz8dgqxLi1Z5Qz2b0OdhkLCzUP62Vb0N74130_assertion description "[Among patients with neonatal diabetes due to KCNJ11 mutations, approximately 25% have neurological findings including developmental delay, motor dysfunction, and epilepsy, known as DEND syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316740.RArZUQgPPJhYz8dgqxLi1Z5Qz2b0OdhkLCzUP62Vb0N74130_provenance.
- NP316740.RArZUQgPPJhYz8dgqxLi1Z5Qz2b0OdhkLCzUP62Vb0N74130_assertion evidence source_evidence_literature NP316740.RArZUQgPPJhYz8dgqxLi1Z5Qz2b0OdhkLCzUP62Vb0N74130_provenance.
- NP316740.RArZUQgPPJhYz8dgqxLi1Z5Qz2b0OdhkLCzUP62Vb0N74130_assertion SIO_000772 19686306 NP316740.RArZUQgPPJhYz8dgqxLi1Z5Qz2b0OdhkLCzUP62Vb0N74130_provenance.
- NP316740.RArZUQgPPJhYz8dgqxLi1Z5Qz2b0OdhkLCzUP62Vb0N74130_assertion wasDerivedFrom befree-20140225 NP316740.RArZUQgPPJhYz8dgqxLi1Z5Qz2b0OdhkLCzUP62Vb0N74130_provenance.
- NP316740.RArZUQgPPJhYz8dgqxLi1Z5Qz2b0OdhkLCzUP62Vb0N74130_assertion wasGeneratedBy ECO_0000203 NP316740.RArZUQgPPJhYz8dgqxLi1Z5Qz2b0OdhkLCzUP62Vb0N74130_provenance.
- befree-20140225 importedOn "2014-02-25" NP316740.RArZUQgPPJhYz8dgqxLi1Z5Qz2b0OdhkLCzUP62Vb0N74130_provenance.