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- source_evidence_literature type ECO_0000212 NP727337.RAB3UEc-0nfqWnLOFMGLRx8QlzGan6Rfa-hULJvJ0Pxk8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP727337.RAB3UEc-0nfqWnLOFMGLRx8QlzGan6Rfa-hULJvJ0Pxk8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP727337.RAB3UEc-0nfqWnLOFMGLRx8QlzGan6Rfa-hULJvJ0Pxk8130_provenance.
- NP727337.RAB3UEc-0nfqWnLOFMGLRx8QlzGan6Rfa-hULJvJ0Pxk8130_assertion description "[Family linkage studies have implicated many chromosomal regions containing RD susceptibility genes, of which putative loci at 1p34-p36 (DYX8), 2p (DYX3), 6p21.3 (DYX2), and 15q21 (DYX1) have been frequently replicated, whereas those at 3p12-q12 (DYX5), 6q13-q16 (DYX4), 11p15 (DYX7), 18p11 (DYX6), and Xq27 (DYX9) have less evidence.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP727337.RAB3UEc-0nfqWnLOFMGLRx8QlzGan6Rfa-hULJvJ0Pxk8130_provenance.
- NP727337.RAB3UEc-0nfqWnLOFMGLRx8QlzGan6Rfa-hULJvJ0Pxk8130_assertion evidence source_evidence_literature NP727337.RAB3UEc-0nfqWnLOFMGLRx8QlzGan6Rfa-hULJvJ0Pxk8130_provenance.
- NP727337.RAB3UEc-0nfqWnLOFMGLRx8QlzGan6Rfa-hULJvJ0Pxk8130_assertion SIO_000772 19302769 NP727337.RAB3UEc-0nfqWnLOFMGLRx8QlzGan6Rfa-hULJvJ0Pxk8130_provenance.
- NP727337.RAB3UEc-0nfqWnLOFMGLRx8QlzGan6Rfa-hULJvJ0Pxk8130_assertion wasDerivedFrom befree-2016 NP727337.RAB3UEc-0nfqWnLOFMGLRx8QlzGan6Rfa-hULJvJ0Pxk8130_provenance.
- NP727337.RAB3UEc-0nfqWnLOFMGLRx8QlzGan6Rfa-hULJvJ0Pxk8130_assertion wasGeneratedBy ECO_0000203 NP727337.RAB3UEc-0nfqWnLOFMGLRx8QlzGan6Rfa-hULJvJ0Pxk8130_provenance.
- befree-2016 importedOn "2016-02-19" NP727337.RAB3UEc-0nfqWnLOFMGLRx8QlzGan6Rfa-hULJvJ0Pxk8130_provenance.