Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1381191.RAk2Y7_3Qho3P7AAvuMkG3eaHwtkHSeT83ShPI_kOn-2w130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1381191.RAk2Y7_3Qho3P7AAvuMkG3eaHwtkHSeT83ShPI_kOn-2w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1381191.RAk2Y7_3Qho3P7AAvuMkG3eaHwtkHSeT83ShPI_kOn-2w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1381191.RAk2Y7_3Qho3P7AAvuMkG3eaHwtkHSeT83ShPI_kOn-2w130_provenance.
- befree-2016 importedOn "2016-02-19" NP1381191.RAk2Y7_3Qho3P7AAvuMkG3eaHwtkHSeT83ShPI_kOn-2w130_provenance.
- NP1381191.RAk2Y7_3Qho3P7AAvuMkG3eaHwtkHSeT83ShPI_kOn-2w130_assertion wasGeneratedBy ECO_0000203 NP1381191.RAk2Y7_3Qho3P7AAvuMkG3eaHwtkHSeT83ShPI_kOn-2w130_provenance.
- NP1381191.RAk2Y7_3Qho3P7AAvuMkG3eaHwtkHSeT83ShPI_kOn-2w130_assertion wasDerivedFrom befree-2016 NP1381191.RAk2Y7_3Qho3P7AAvuMkG3eaHwtkHSeT83ShPI_kOn-2w130_provenance.
- NP1381191.RAk2Y7_3Qho3P7AAvuMkG3eaHwtkHSeT83ShPI_kOn-2w130_assertion SIO_000772 9313763 NP1381191.RAk2Y7_3Qho3P7AAvuMkG3eaHwtkHSeT83ShPI_kOn-2w130_provenance.
- NP1381191.RAk2Y7_3Qho3P7AAvuMkG3eaHwtkHSeT83ShPI_kOn-2w130_assertion evidence source_evidence_literature NP1381191.RAk2Y7_3Qho3P7AAvuMkG3eaHwtkHSeT83ShPI_kOn-2w130_provenance.
- NP1381191.RAk2Y7_3Qho3P7AAvuMkG3eaHwtkHSeT83ShPI_kOn-2w130_assertion description "[A frameshift mutation of P291 fsinsC (insertion of a C in a polyC tract around codon 291 for Pro), which would generate a mutant truncated protein of 340 amino acids, was found in a subject who started insulin treatment when hyperglycemia and ketonuria were noticed at 13 years of age.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1381191.RAk2Y7_3Qho3P7AAvuMkG3eaHwtkHSeT83ShPI_kOn-2w130_provenance.