Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1007768.RAQFMa5xmAqy4Gg1VUAJMCq8FoxiXGRaB3Pn_5UIy6VeA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1007768.RAQFMa5xmAqy4Gg1VUAJMCq8FoxiXGRaB3Pn_5UIy6VeA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1007768.RAQFMa5xmAqy4Gg1VUAJMCq8FoxiXGRaB3Pn_5UIy6VeA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1007768.RAQFMa5xmAqy4Gg1VUAJMCq8FoxiXGRaB3Pn_5UIy6VeA130_provenance.
- NP1007768.RAQFMa5xmAqy4Gg1VUAJMCq8FoxiXGRaB3Pn_5UIy6VeA130_assertion description "[We report a homozygous missense mutation at position 1092 (substitution of glutamine for arginine) in the tyrosine kinase domain of the insulin receptor in a patient with leprechaunism associated with severe insulin resistance and intrauterine growth retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1007768.RAQFMa5xmAqy4Gg1VUAJMCq8FoxiXGRaB3Pn_5UIy6VeA130_provenance.
- NP1007768.RAQFMa5xmAqy4Gg1VUAJMCq8FoxiXGRaB3Pn_5UIy6VeA130_assertion evidence source_evidence_literature NP1007768.RAQFMa5xmAqy4Gg1VUAJMCq8FoxiXGRaB3Pn_5UIy6VeA130_provenance.
- NP1007768.RAQFMa5xmAqy4Gg1VUAJMCq8FoxiXGRaB3Pn_5UIy6VeA130_assertion SIO_000772 9112018 NP1007768.RAQFMa5xmAqy4Gg1VUAJMCq8FoxiXGRaB3Pn_5UIy6VeA130_provenance.
- NP1007768.RAQFMa5xmAqy4Gg1VUAJMCq8FoxiXGRaB3Pn_5UIy6VeA130_assertion wasDerivedFrom befree-20150227 NP1007768.RAQFMa5xmAqy4Gg1VUAJMCq8FoxiXGRaB3Pn_5UIy6VeA130_provenance.
- NP1007768.RAQFMa5xmAqy4Gg1VUAJMCq8FoxiXGRaB3Pn_5UIy6VeA130_assertion wasGeneratedBy ECO_0000203 NP1007768.RAQFMa5xmAqy4Gg1VUAJMCq8FoxiXGRaB3Pn_5UIy6VeA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP1007768.RAQFMa5xmAqy4Gg1VUAJMCq8FoxiXGRaB3Pn_5UIy6VeA130_provenance.