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- source_evidence_literature type ECO_0000212 NP724933.RAnMb6WJ2mMYl4nhLK0WmvizdnMSNjk0dviYbf-gzVywM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP724933.RAnMb6WJ2mMYl4nhLK0WmvizdnMSNjk0dviYbf-gzVywM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP724933.RAnMb6WJ2mMYl4nhLK0WmvizdnMSNjk0dviYbf-gzVywM130_provenance.
- NP724933.RAnMb6WJ2mMYl4nhLK0WmvizdnMSNjk0dviYbf-gzVywM130_assertion description "[Novel presentations of congenital hyperinsulinism due to mutations in the MODY genes: HNF1A and HNF4A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP724933.RAnMb6WJ2mMYl4nhLK0WmvizdnMSNjk0dviYbf-gzVywM130_provenance.
- NP724933.RAnMb6WJ2mMYl4nhLK0WmvizdnMSNjk0dviYbf-gzVywM130_assertion evidence source_evidence_literature NP724933.RAnMb6WJ2mMYl4nhLK0WmvizdnMSNjk0dviYbf-gzVywM130_provenance.
- NP724933.RAnMb6WJ2mMYl4nhLK0WmvizdnMSNjk0dviYbf-gzVywM130_assertion SIO_000772 22802087 NP724933.RAnMb6WJ2mMYl4nhLK0WmvizdnMSNjk0dviYbf-gzVywM130_provenance.
- NP724933.RAnMb6WJ2mMYl4nhLK0WmvizdnMSNjk0dviYbf-gzVywM130_assertion wasDerivedFrom befree-20150227 NP724933.RAnMb6WJ2mMYl4nhLK0WmvizdnMSNjk0dviYbf-gzVywM130_provenance.
- NP724933.RAnMb6WJ2mMYl4nhLK0WmvizdnMSNjk0dviYbf-gzVywM130_assertion wasGeneratedBy ECO_0000203 NP724933.RAnMb6WJ2mMYl4nhLK0WmvizdnMSNjk0dviYbf-gzVywM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP724933.RAnMb6WJ2mMYl4nhLK0WmvizdnMSNjk0dviYbf-gzVywM130_provenance.