Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP615925.RAQ61u9XsMjVWQMW9G61LTJ0QWZTsEwGgWyZsaL9TriBU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP615925.RAQ61u9XsMjVWQMW9G61LTJ0QWZTsEwGgWyZsaL9TriBU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP615925.RAQ61u9XsMjVWQMW9G61LTJ0QWZTsEwGgWyZsaL9TriBU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP615925.RAQ61u9XsMjVWQMW9G61LTJ0QWZTsEwGgWyZsaL9TriBU130_provenance.
- NP615925.RAQ61u9XsMjVWQMW9G61LTJ0QWZTsEwGgWyZsaL9TriBU130_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." NP615925.RAQ61u9XsMjVWQMW9G61LTJ0QWZTsEwGgWyZsaL9TriBU130_provenance.
- NP615925.RAQ61u9XsMjVWQMW9G61LTJ0QWZTsEwGgWyZsaL9TriBU130_assertion evidence source_evidence_literature NP615925.RAQ61u9XsMjVWQMW9G61LTJ0QWZTsEwGgWyZsaL9TriBU130_provenance.
- NP615925.RAQ61u9XsMjVWQMW9G61LTJ0QWZTsEwGgWyZsaL9TriBU130_assertion SIO_000772 9313763 NP615925.RAQ61u9XsMjVWQMW9G61LTJ0QWZTsEwGgWyZsaL9TriBU130_provenance.
- NP615925.RAQ61u9XsMjVWQMW9G61LTJ0QWZTsEwGgWyZsaL9TriBU130_assertion wasDerivedFrom befree-20140225 NP615925.RAQ61u9XsMjVWQMW9G61LTJ0QWZTsEwGgWyZsaL9TriBU130_provenance.
- NP615925.RAQ61u9XsMjVWQMW9G61LTJ0QWZTsEwGgWyZsaL9TriBU130_assertion wasGeneratedBy ECO_0000203 NP615925.RAQ61u9XsMjVWQMW9G61LTJ0QWZTsEwGgWyZsaL9TriBU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP615925.RAQ61u9XsMjVWQMW9G61LTJ0QWZTsEwGgWyZsaL9TriBU130_provenance.