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- NP574226.RAYWF-5bzPeNAaD9AFZfQVIlB-w9Yc7CivZNjS77Nn1XY130_assertion type Assertion NP574226.RAYWF-5bzPeNAaD9AFZfQVIlB-w9Yc7CivZNjS77Nn1XY130_head.
- NP574226.RAYWF-5bzPeNAaD9AFZfQVIlB-w9Yc7CivZNjS77Nn1XY130_assertion wasGeneratedBy ECO_0000203 NP574226.RAYWF-5bzPeNAaD9AFZfQVIlB-w9Yc7CivZNjS77Nn1XY130_provenance.
- NP574226.RAYWF-5bzPeNAaD9AFZfQVIlB-w9Yc7CivZNjS77Nn1XY130_assertion wasDerivedFrom befree-20150227 NP574226.RAYWF-5bzPeNAaD9AFZfQVIlB-w9Yc7CivZNjS77Nn1XY130_provenance.
- NP574226.RAYWF-5bzPeNAaD9AFZfQVIlB-w9Yc7CivZNjS77Nn1XY130_assertion SIO_000772 21355073 NP574226.RAYWF-5bzPeNAaD9AFZfQVIlB-w9Yc7CivZNjS77Nn1XY130_provenance.
- NP574226.RAYWF-5bzPeNAaD9AFZfQVIlB-w9Yc7CivZNjS77Nn1XY130_assertion evidence source_evidence_literature NP574226.RAYWF-5bzPeNAaD9AFZfQVIlB-w9Yc7CivZNjS77Nn1XY130_provenance.
- NP574226.RAYWF-5bzPeNAaD9AFZfQVIlB-w9Yc7CivZNjS77Nn1XY130_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." NP574226.RAYWF-5bzPeNAaD9AFZfQVIlB-w9Yc7CivZNjS77Nn1XY130_provenance.