Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1008497.RA5ClBcNMyJheKAjStqzPECNW_7MlvV5YmEb4e3zdUbPw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1008497.RA5ClBcNMyJheKAjStqzPECNW_7MlvV5YmEb4e3zdUbPw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1008497.RA5ClBcNMyJheKAjStqzPECNW_7MlvV5YmEb4e3zdUbPw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1008497.RA5ClBcNMyJheKAjStqzPECNW_7MlvV5YmEb4e3zdUbPw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP1008497.RA5ClBcNMyJheKAjStqzPECNW_7MlvV5YmEb4e3zdUbPw130_provenance.
- NP1008497.RA5ClBcNMyJheKAjStqzPECNW_7MlvV5YmEb4e3zdUbPw130_assertion wasGeneratedBy ECO_0000203 NP1008497.RA5ClBcNMyJheKAjStqzPECNW_7MlvV5YmEb4e3zdUbPw130_provenance.
- NP1008497.RA5ClBcNMyJheKAjStqzPECNW_7MlvV5YmEb4e3zdUbPw130_assertion wasDerivedFrom befree-20150227 NP1008497.RA5ClBcNMyJheKAjStqzPECNW_7MlvV5YmEb4e3zdUbPw130_provenance.
- NP1008497.RA5ClBcNMyJheKAjStqzPECNW_7MlvV5YmEb4e3zdUbPw130_assertion SIO_000772 8923010 NP1008497.RA5ClBcNMyJheKAjStqzPECNW_7MlvV5YmEb4e3zdUbPw130_provenance.
- NP1008497.RA5ClBcNMyJheKAjStqzPECNW_7MlvV5YmEb4e3zdUbPw130_assertion evidence source_evidence_literature NP1008497.RA5ClBcNMyJheKAjStqzPECNW_7MlvV5YmEb4e3zdUbPw130_provenance.
- NP1008497.RA5ClBcNMyJheKAjStqzPECNW_7MlvV5YmEb4e3zdUbPw130_assertion description "[Mutations in SUR have been identified in individuals affected with familial persistent hyper-insulinemic hypoglycemia of infancy (PHHI), an autosomal recessive disorder of glucose metabolism which is linked to chromosome 11p15.1 and characterized by unregulated secretion of insulin and profound hypoglycemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1008497.RA5ClBcNMyJheKAjStqzPECNW_7MlvV5YmEb4e3zdUbPw130_provenance.