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- source_evidence_literature type ECO_0000212 NP1074849.RARuThYr1LxBqeXZxCk9Cq5F7cZnAGET_ctqwNqKb_3xo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1074849.RARuThYr1LxBqeXZxCk9Cq5F7cZnAGET_ctqwNqKb_3xo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1074849.RARuThYr1LxBqeXZxCk9Cq5F7cZnAGET_ctqwNqKb_3xo130_provenance.
- NP1074849.RARuThYr1LxBqeXZxCk9Cq5F7cZnAGET_ctqwNqKb_3xo130_assertion description "[High frequency of NAD(P)H:quinone oxidoreductase 1 (NQO1) C(609)T germline polymorphism in MDS/AML with trisomy 8.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1074849.RARuThYr1LxBqeXZxCk9Cq5F7cZnAGET_ctqwNqKb_3xo130_provenance.
- NP1074849.RARuThYr1LxBqeXZxCk9Cq5F7cZnAGET_ctqwNqKb_3xo130_assertion evidence source_evidence_literature NP1074849.RARuThYr1LxBqeXZxCk9Cq5F7cZnAGET_ctqwNqKb_3xo130_provenance.
- NP1074849.RARuThYr1LxBqeXZxCk9Cq5F7cZnAGET_ctqwNqKb_3xo130_assertion SIO_000772 23643325 NP1074849.RARuThYr1LxBqeXZxCk9Cq5F7cZnAGET_ctqwNqKb_3xo130_provenance.
- NP1074849.RARuThYr1LxBqeXZxCk9Cq5F7cZnAGET_ctqwNqKb_3xo130_assertion wasDerivedFrom befree-2016 NP1074849.RARuThYr1LxBqeXZxCk9Cq5F7cZnAGET_ctqwNqKb_3xo130_provenance.
- NP1074849.RARuThYr1LxBqeXZxCk9Cq5F7cZnAGET_ctqwNqKb_3xo130_assertion wasGeneratedBy ECO_0000203 NP1074849.RARuThYr1LxBqeXZxCk9Cq5F7cZnAGET_ctqwNqKb_3xo130_provenance.
- befree-2016 importedOn "2016-02-19" NP1074849.RARuThYr1LxBqeXZxCk9Cq5F7cZnAGET_ctqwNqKb_3xo130_provenance.