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- source_evidence_literature type ECO_0000212 NP493060.RA91rZ1njqySvL6lMW77_feQsQQL67a2Frc_d8q2DY29g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP493060.RA91rZ1njqySvL6lMW77_feQsQQL67a2Frc_d8q2DY29g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP493060.RA91rZ1njqySvL6lMW77_feQsQQL67a2Frc_d8q2DY29g130_provenance.
- NP493060.RA91rZ1njqySvL6lMW77_feQsQQL67a2Frc_d8q2DY29g130_assertion description "[Hyperinsulinism of infancy associated with a novel splice site mutation in the SCHAD gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP493060.RA91rZ1njqySvL6lMW77_feQsQQL67a2Frc_d8q2DY29g130_provenance.
- NP493060.RA91rZ1njqySvL6lMW77_feQsQQL67a2Frc_d8q2DY29g130_assertion evidence source_evidence_literature NP493060.RA91rZ1njqySvL6lMW77_feQsQQL67a2Frc_d8q2DY29g130_provenance.
- NP493060.RA91rZ1njqySvL6lMW77_feQsQQL67a2Frc_d8q2DY29g130_assertion SIO_000772 15870679 NP493060.RA91rZ1njqySvL6lMW77_feQsQQL67a2Frc_d8q2DY29g130_provenance.
- NP493060.RA91rZ1njqySvL6lMW77_feQsQQL67a2Frc_d8q2DY29g130_assertion wasDerivedFrom befree-2016 NP493060.RA91rZ1njqySvL6lMW77_feQsQQL67a2Frc_d8q2DY29g130_provenance.
- NP493060.RA91rZ1njqySvL6lMW77_feQsQQL67a2Frc_d8q2DY29g130_assertion wasGeneratedBy ECO_0000203 NP493060.RA91rZ1njqySvL6lMW77_feQsQQL67a2Frc_d8q2DY29g130_provenance.
- befree-2016 importedOn "2016-02-19" NP493060.RA91rZ1njqySvL6lMW77_feQsQQL67a2Frc_d8q2DY29g130_provenance.