Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP665718.RAHQlYY9qbBL8oiyQmfeWNY-Vy2PEc-TmNjAKPrtnk4oc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP665718.RAHQlYY9qbBL8oiyQmfeWNY-Vy2PEc-TmNjAKPrtnk4oc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP665718.RAHQlYY9qbBL8oiyQmfeWNY-Vy2PEc-TmNjAKPrtnk4oc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP665718.RAHQlYY9qbBL8oiyQmfeWNY-Vy2PEc-TmNjAKPrtnk4oc130_provenance.
- NP665718.RAHQlYY9qbBL8oiyQmfeWNY-Vy2PEc-TmNjAKPrtnk4oc130_assertion description "[Homozygous or compound heterozygous mutations within the insulin binding domain of the human insulin receptor (INSR) are usually associated with severe impairment of insulin binding leading to Donohue syndrome (Leprechaunism), which is characterized by excessive hyperglycemia with hyperinsulinism, pre- and postnatal growth retardation, distinct dysmorphism and early death.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP665718.RAHQlYY9qbBL8oiyQmfeWNY-Vy2PEc-TmNjAKPrtnk4oc130_provenance.
- NP665718.RAHQlYY9qbBL8oiyQmfeWNY-Vy2PEc-TmNjAKPrtnk4oc130_assertion evidence source_evidence_literature NP665718.RAHQlYY9qbBL8oiyQmfeWNY-Vy2PEc-TmNjAKPrtnk4oc130_provenance.
- NP665718.RAHQlYY9qbBL8oiyQmfeWNY-Vy2PEc-TmNjAKPrtnk4oc130_assertion SIO_000772 18411068 NP665718.RAHQlYY9qbBL8oiyQmfeWNY-Vy2PEc-TmNjAKPrtnk4oc130_provenance.
- NP665718.RAHQlYY9qbBL8oiyQmfeWNY-Vy2PEc-TmNjAKPrtnk4oc130_assertion wasDerivedFrom befree-2016 NP665718.RAHQlYY9qbBL8oiyQmfeWNY-Vy2PEc-TmNjAKPrtnk4oc130_provenance.
- NP665718.RAHQlYY9qbBL8oiyQmfeWNY-Vy2PEc-TmNjAKPrtnk4oc130_assertion wasGeneratedBy ECO_0000203 NP665718.RAHQlYY9qbBL8oiyQmfeWNY-Vy2PEc-TmNjAKPrtnk4oc130_provenance.
- befree-2016 importedOn "2016-02-19" NP665718.RAHQlYY9qbBL8oiyQmfeWNY-Vy2PEc-TmNjAKPrtnk4oc130_provenance.