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- source_evidence_literature type ECO_0000212 NP186106.RAm6H5YsD0FcUcYnWbCjFDmC8zaGE2hx23aUuAdoXa0kg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP186106.RAm6H5YsD0FcUcYnWbCjFDmC8zaGE2hx23aUuAdoXa0kg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP186106.RAm6H5YsD0FcUcYnWbCjFDmC8zaGE2hx23aUuAdoXa0kg130_provenance.
- NP186106.RAm6H5YsD0FcUcYnWbCjFDmC8zaGE2hx23aUuAdoXa0kg130_assertion description "[The authors present here the clinical, anatomic, and endocrine-metabolic studies of three patients, with a view toward careful delineation of the syndrome and further characterization of the metabolic defect.The most striking and consistent metabolic derangements present in all of these patients were fasting hypoglycemia (less than 20 mg/dL), postprandial hyperglycemia (more than 250 mg/dL), marked hyperinsulinemia (more than 2000 ?U/mL), and severe insulin resistance (less than a 20 percent decrease in blood sugar with 0.3 to 1.0 U/kg of regular insulin IV).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186106.RAm6H5YsD0FcUcYnWbCjFDmC8zaGE2hx23aUuAdoXa0kg130_provenance.
- NP186106.RAm6H5YsD0FcUcYnWbCjFDmC8zaGE2hx23aUuAdoXa0kg130_assertion evidence source_evidence_literature NP186106.RAm6H5YsD0FcUcYnWbCjFDmC8zaGE2hx23aUuAdoXa0kg130_provenance.
- NP186106.RAm6H5YsD0FcUcYnWbCjFDmC8zaGE2hx23aUuAdoXa0kg130_assertion SIO_000772 7154104 NP186106.RAm6H5YsD0FcUcYnWbCjFDmC8zaGE2hx23aUuAdoXa0kg130_provenance.
- NP186106.RAm6H5YsD0FcUcYnWbCjFDmC8zaGE2hx23aUuAdoXa0kg130_assertion wasDerivedFrom befree-20140225 NP186106.RAm6H5YsD0FcUcYnWbCjFDmC8zaGE2hx23aUuAdoXa0kg130_provenance.
- NP186106.RAm6H5YsD0FcUcYnWbCjFDmC8zaGE2hx23aUuAdoXa0kg130_assertion wasGeneratedBy ECO_0000203 NP186106.RAm6H5YsD0FcUcYnWbCjFDmC8zaGE2hx23aUuAdoXa0kg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP186106.RAm6H5YsD0FcUcYnWbCjFDmC8zaGE2hx23aUuAdoXa0kg130_provenance.