Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP574226.RAYWF-5bzPeNAaD9AFZfQVIlB-w9Yc7CivZNjS77Nn1XY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP574226.RAYWF-5bzPeNAaD9AFZfQVIlB-w9Yc7CivZNjS77Nn1XY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP574226.RAYWF-5bzPeNAaD9AFZfQVIlB-w9Yc7CivZNjS77Nn1XY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP574226.RAYWF-5bzPeNAaD9AFZfQVIlB-w9Yc7CivZNjS77Nn1XY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP574226.RAYWF-5bzPeNAaD9AFZfQVIlB-w9Yc7CivZNjS77Nn1XY130_provenance.
- 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.