Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP540902.RA6gCB8wVu_-_iFfpEF3eofVgjfyH2AdI8DSFuSNdg4qM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP540902.RA6gCB8wVu_-_iFfpEF3eofVgjfyH2AdI8DSFuSNdg4qM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP540902.RA6gCB8wVu_-_iFfpEF3eofVgjfyH2AdI8DSFuSNdg4qM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP540902.RA6gCB8wVu_-_iFfpEF3eofVgjfyH2AdI8DSFuSNdg4qM130_provenance.
- NP540902.RA6gCB8wVu_-_iFfpEF3eofVgjfyH2AdI8DSFuSNdg4qM130_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." NP540902.RA6gCB8wVu_-_iFfpEF3eofVgjfyH2AdI8DSFuSNdg4qM130_provenance.
- NP540902.RA6gCB8wVu_-_iFfpEF3eofVgjfyH2AdI8DSFuSNdg4qM130_assertion evidence source_evidence_literature NP540902.RA6gCB8wVu_-_iFfpEF3eofVgjfyH2AdI8DSFuSNdg4qM130_provenance.
- NP540902.RA6gCB8wVu_-_iFfpEF3eofVgjfyH2AdI8DSFuSNdg4qM130_assertion SIO_000772 18411068 NP540902.RA6gCB8wVu_-_iFfpEF3eofVgjfyH2AdI8DSFuSNdg4qM130_provenance.
- NP540902.RA6gCB8wVu_-_iFfpEF3eofVgjfyH2AdI8DSFuSNdg4qM130_assertion wasDerivedFrom befree-20140225 NP540902.RA6gCB8wVu_-_iFfpEF3eofVgjfyH2AdI8DSFuSNdg4qM130_provenance.
- NP540902.RA6gCB8wVu_-_iFfpEF3eofVgjfyH2AdI8DSFuSNdg4qM130_assertion wasGeneratedBy ECO_0000203 NP540902.RA6gCB8wVu_-_iFfpEF3eofVgjfyH2AdI8DSFuSNdg4qM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP540902.RA6gCB8wVu_-_iFfpEF3eofVgjfyH2AdI8DSFuSNdg4qM130_provenance.