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- NP875485.RA0Ne81dKzhI0C_rNeKkNnVn7-rxWqGYUE5WnqbX2obrk130_assertion type Assertion NP875485.RA0Ne81dKzhI0C_rNeKkNnVn7-rxWqGYUE5WnqbX2obrk130_head.
- NP875485.RA0Ne81dKzhI0C_rNeKkNnVn7-rxWqGYUE5WnqbX2obrk130_assertion wasGeneratedBy ECO_0000203 NP875485.RA0Ne81dKzhI0C_rNeKkNnVn7-rxWqGYUE5WnqbX2obrk130_provenance.
- NP875485.RA0Ne81dKzhI0C_rNeKkNnVn7-rxWqGYUE5WnqbX2obrk130_assertion wasDerivedFrom befree-2016 NP875485.RA0Ne81dKzhI0C_rNeKkNnVn7-rxWqGYUE5WnqbX2obrk130_provenance.
- NP875485.RA0Ne81dKzhI0C_rNeKkNnVn7-rxWqGYUE5WnqbX2obrk130_assertion SIO_000772 21355073 NP875485.RA0Ne81dKzhI0C_rNeKkNnVn7-rxWqGYUE5WnqbX2obrk130_provenance.
- NP875485.RA0Ne81dKzhI0C_rNeKkNnVn7-rxWqGYUE5WnqbX2obrk130_assertion evidence source_evidence_literature NP875485.RA0Ne81dKzhI0C_rNeKkNnVn7-rxWqGYUE5WnqbX2obrk130_provenance.
- NP875485.RA0Ne81dKzhI0C_rNeKkNnVn7-rxWqGYUE5WnqbX2obrk130_assertion description "[Two rare variants (OGG1 c.137G>A; MUTYH c.1187G>A) and one common polymorphism (NUDT1 c.426C>T) were associated with CRC risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP875485.RA0Ne81dKzhI0C_rNeKkNnVn7-rxWqGYUE5WnqbX2obrk130_provenance.