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- source_evidence_literature type ECO_0000212 NP343256.RA3MIFUVMKnzX4KEO9FDQqr42d0W-TFD75dZsrJO2aJus130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP343256.RA3MIFUVMKnzX4KEO9FDQqr42d0W-TFD75dZsrJO2aJus130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP343256.RA3MIFUVMKnzX4KEO9FDQqr42d0W-TFD75dZsrJO2aJus130_provenance.
- NP343256.RA3MIFUVMKnzX4KEO9FDQqr42d0W-TFD75dZsrJO2aJus130_assertion description "[Thus, our results confirm that mutations of SLC2A2 are the basic defect in patients with FBS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP343256.RA3MIFUVMKnzX4KEO9FDQqr42d0W-TFD75dZsrJO2aJus130_provenance.
- NP343256.RA3MIFUVMKnzX4KEO9FDQqr42d0W-TFD75dZsrJO2aJus130_assertion evidence source_evidence_literature NP343256.RA3MIFUVMKnzX4KEO9FDQqr42d0W-TFD75dZsrJO2aJus130_provenance.
- NP343256.RA3MIFUVMKnzX4KEO9FDQqr42d0W-TFD75dZsrJO2aJus130_assertion SIO_000772 11810292 NP343256.RA3MIFUVMKnzX4KEO9FDQqr42d0W-TFD75dZsrJO2aJus130_provenance.
- NP343256.RA3MIFUVMKnzX4KEO9FDQqr42d0W-TFD75dZsrJO2aJus130_assertion wasDerivedFrom befree-2016 NP343256.RA3MIFUVMKnzX4KEO9FDQqr42d0W-TFD75dZsrJO2aJus130_provenance.
- NP343256.RA3MIFUVMKnzX4KEO9FDQqr42d0W-TFD75dZsrJO2aJus130_assertion wasGeneratedBy ECO_0000203 NP343256.RA3MIFUVMKnzX4KEO9FDQqr42d0W-TFD75dZsrJO2aJus130_provenance.
- befree-2016 importedOn "2016-02-19" NP343256.RA3MIFUVMKnzX4KEO9FDQqr42d0W-TFD75dZsrJO2aJus130_provenance.