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- source_evidence_literature type ECO_0000212 NP1232515.RAPG1Zo0K-sGR1EMlkF3XglBpT2rnsc5Mwbeo3C1CfLYc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1232515.RAPG1Zo0K-sGR1EMlkF3XglBpT2rnsc5Mwbeo3C1CfLYc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1232515.RAPG1Zo0K-sGR1EMlkF3XglBpT2rnsc5Mwbeo3C1CfLYc130_provenance.
- NP1232515.RAPG1Zo0K-sGR1EMlkF3XglBpT2rnsc5Mwbeo3C1CfLYc130_assertion description "[KCNJ1 variation is associated with multiple diseases, such as antenatal Bartter syndrome and diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1232515.RAPG1Zo0K-sGR1EMlkF3XglBpT2rnsc5Mwbeo3C1CfLYc130_provenance.
- NP1232515.RAPG1Zo0K-sGR1EMlkF3XglBpT2rnsc5Mwbeo3C1CfLYc130_assertion evidence source_evidence_literature NP1232515.RAPG1Zo0K-sGR1EMlkF3XglBpT2rnsc5Mwbeo3C1CfLYc130_provenance.
- NP1232515.RAPG1Zo0K-sGR1EMlkF3XglBpT2rnsc5Mwbeo3C1CfLYc130_assertion SIO_000772 25344677 NP1232515.RAPG1Zo0K-sGR1EMlkF3XglBpT2rnsc5Mwbeo3C1CfLYc130_provenance.
- NP1232515.RAPG1Zo0K-sGR1EMlkF3XglBpT2rnsc5Mwbeo3C1CfLYc130_assertion wasDerivedFrom befree-2016 NP1232515.RAPG1Zo0K-sGR1EMlkF3XglBpT2rnsc5Mwbeo3C1CfLYc130_provenance.
- NP1232515.RAPG1Zo0K-sGR1EMlkF3XglBpT2rnsc5Mwbeo3C1CfLYc130_assertion wasGeneratedBy ECO_0000203 NP1232515.RAPG1Zo0K-sGR1EMlkF3XglBpT2rnsc5Mwbeo3C1CfLYc130_provenance.
- befree-2016 importedOn "2016-02-19" NP1232515.RAPG1Zo0K-sGR1EMlkF3XglBpT2rnsc5Mwbeo3C1CfLYc130_provenance.