Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP420918.RAGN2zMD9GEY9FJMS6SDL1OOTgIutrScbwptqmrYsxhoo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP420918.RAGN2zMD9GEY9FJMS6SDL1OOTgIutrScbwptqmrYsxhoo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP420918.RAGN2zMD9GEY9FJMS6SDL1OOTgIutrScbwptqmrYsxhoo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP420918.RAGN2zMD9GEY9FJMS6SDL1OOTgIutrScbwptqmrYsxhoo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP420918.RAGN2zMD9GEY9FJMS6SDL1OOTgIutrScbwptqmrYsxhoo130_provenance.
- NP420918.RAGN2zMD9GEY9FJMS6SDL1OOTgIutrScbwptqmrYsxhoo130_assertion wasGeneratedBy ECO_0000203 NP420918.RAGN2zMD9GEY9FJMS6SDL1OOTgIutrScbwptqmrYsxhoo130_provenance.
- NP420918.RAGN2zMD9GEY9FJMS6SDL1OOTgIutrScbwptqmrYsxhoo130_assertion wasDerivedFrom befree-20150227 NP420918.RAGN2zMD9GEY9FJMS6SDL1OOTgIutrScbwptqmrYsxhoo130_provenance.
- NP420918.RAGN2zMD9GEY9FJMS6SDL1OOTgIutrScbwptqmrYsxhoo130_assertion SIO_000772 19146401 NP420918.RAGN2zMD9GEY9FJMS6SDL1OOTgIutrScbwptqmrYsxhoo130_provenance.
- NP420918.RAGN2zMD9GEY9FJMS6SDL1OOTgIutrScbwptqmrYsxhoo130_assertion evidence source_evidence_literature NP420918.RAGN2zMD9GEY9FJMS6SDL1OOTgIutrScbwptqmrYsxhoo130_provenance.
- NP420918.RAGN2zMD9GEY9FJMS6SDL1OOTgIutrScbwptqmrYsxhoo130_assertion description "[We describe the discovery of 11 new activating mutations in the human glk gene associated with the disease persistent hyperinsulinemic hypoglycemia of infancy (PHHI).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP420918.RAGN2zMD9GEY9FJMS6SDL1OOTgIutrScbwptqmrYsxhoo130_provenance.