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- source_evidence_literature type ECO_0000212 NP883078.RAqG1MAZ-Yh11XUtn94XVSXEUINTlSeIOo1eeU9DKkYd4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP883078.RAqG1MAZ-Yh11XUtn94XVSXEUINTlSeIOo1eeU9DKkYd4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP883078.RAqG1MAZ-Yh11XUtn94XVSXEUINTlSeIOo1eeU9DKkYd4130_provenance.
- NP883078.RAqG1MAZ-Yh11XUtn94XVSXEUINTlSeIOo1eeU9DKkYd4130_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." NP883078.RAqG1MAZ-Yh11XUtn94XVSXEUINTlSeIOo1eeU9DKkYd4130_provenance.
- NP883078.RAqG1MAZ-Yh11XUtn94XVSXEUINTlSeIOo1eeU9DKkYd4130_assertion evidence source_evidence_literature NP883078.RAqG1MAZ-Yh11XUtn94XVSXEUINTlSeIOo1eeU9DKkYd4130_provenance.
- NP883078.RAqG1MAZ-Yh11XUtn94XVSXEUINTlSeIOo1eeU9DKkYd4130_assertion SIO_000772 19302769 NP883078.RAqG1MAZ-Yh11XUtn94XVSXEUINTlSeIOo1eeU9DKkYd4130_provenance.
- NP883078.RAqG1MAZ-Yh11XUtn94XVSXEUINTlSeIOo1eeU9DKkYd4130_assertion wasDerivedFrom befree-20150227 NP883078.RAqG1MAZ-Yh11XUtn94XVSXEUINTlSeIOo1eeU9DKkYd4130_provenance.
- NP883078.RAqG1MAZ-Yh11XUtn94XVSXEUINTlSeIOo1eeU9DKkYd4130_assertion wasGeneratedBy ECO_0000203 NP883078.RAqG1MAZ-Yh11XUtn94XVSXEUINTlSeIOo1eeU9DKkYd4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP883078.RAqG1MAZ-Yh11XUtn94XVSXEUINTlSeIOo1eeU9DKkYd4130_provenance.