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- NP185280.RAaSfFNB2I5okAqFpUyETevExVP6x0VCvQx_jwYJQVWkg130_assertion type Assertion NP185280.RAaSfFNB2I5okAqFpUyETevExVP6x0VCvQx_jwYJQVWkg130_head.
- NP185280.RAaSfFNB2I5okAqFpUyETevExVP6x0VCvQx_jwYJQVWkg130_assertion wasGeneratedBy ECO_0000203 NP185280.RAaSfFNB2I5okAqFpUyETevExVP6x0VCvQx_jwYJQVWkg130_provenance.
- NP185280.RAaSfFNB2I5okAqFpUyETevExVP6x0VCvQx_jwYJQVWkg130_assertion wasDerivedFrom befree-20140225 NP185280.RAaSfFNB2I5okAqFpUyETevExVP6x0VCvQx_jwYJQVWkg130_provenance.
- NP185280.RAaSfFNB2I5okAqFpUyETevExVP6x0VCvQx_jwYJQVWkg130_assertion SIO_000772 15161766 NP185280.RAaSfFNB2I5okAqFpUyETevExVP6x0VCvQx_jwYJQVWkg130_provenance.
- NP185280.RAaSfFNB2I5okAqFpUyETevExVP6x0VCvQx_jwYJQVWkg130_assertion evidence source_evidence_literature NP185280.RAaSfFNB2I5okAqFpUyETevExVP6x0VCvQx_jwYJQVWkg130_provenance.
- NP185280.RAaSfFNB2I5okAqFpUyETevExVP6x0VCvQx_jwYJQVWkg130_assertion description "[A novel syndrome of autosomal-dominant hyperinsulinemic hypoglycemia linked to a mutation in the human insulin receptor gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185280.RAaSfFNB2I5okAqFpUyETevExVP6x0VCvQx_jwYJQVWkg130_provenance.