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- source_evidence_literature type ECO_0000212 NP450500.RACIAk10CBeJTSXjFT5i2mGh-8-tEV6ds7GeryleKjs4A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP450500.RACIAk10CBeJTSXjFT5i2mGh-8-tEV6ds7GeryleKjs4A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP450500.RACIAk10CBeJTSXjFT5i2mGh-8-tEV6ds7GeryleKjs4A130_provenance.
- NP450500.RACIAk10CBeJTSXjFT5i2mGh-8-tEV6ds7GeryleKjs4A130_assertion description "[To investigate the prevalence of potential mutations in the gene encoding HKII, we used the polymerase chain reaction (PCR) to amplify each of the 18 exons of the HKII gene from genomic DNA derived from 59 subjects: 25 insulin-resistant probands with clinical features of the type A syndrome and 34 NIDDM subjects enrolled in the United Kingdom Prospective Study of Therapies of NIDDM (UKPDS) who represented the highest percentile of fasting hyperinsulinemia in the UKPDS population of 5,098 subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP450500.RACIAk10CBeJTSXjFT5i2mGh-8-tEV6ds7GeryleKjs4A130_provenance.
- NP450500.RACIAk10CBeJTSXjFT5i2mGh-8-tEV6ds7GeryleKjs4A130_assertion evidence source_evidence_literature NP450500.RACIAk10CBeJTSXjFT5i2mGh-8-tEV6ds7GeryleKjs4A130_provenance.
- NP450500.RACIAk10CBeJTSXjFT5i2mGh-8-tEV6ds7GeryleKjs4A130_assertion SIO_000772 7883122 NP450500.RACIAk10CBeJTSXjFT5i2mGh-8-tEV6ds7GeryleKjs4A130_provenance.
- NP450500.RACIAk10CBeJTSXjFT5i2mGh-8-tEV6ds7GeryleKjs4A130_assertion wasDerivedFrom befree-20150227 NP450500.RACIAk10CBeJTSXjFT5i2mGh-8-tEV6ds7GeryleKjs4A130_provenance.
- NP450500.RACIAk10CBeJTSXjFT5i2mGh-8-tEV6ds7GeryleKjs4A130_assertion wasGeneratedBy ECO_0000203 NP450500.RACIAk10CBeJTSXjFT5i2mGh-8-tEV6ds7GeryleKjs4A130_provenance.
- befree-20150227 importedOn "2015-02-27" NP450500.RACIAk10CBeJTSXjFT5i2mGh-8-tEV6ds7GeryleKjs4A130_provenance.