Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP602381.RAvWo3ifV7h5GrOO40W-1h7zvj6vbBFQ94mkUqpTe3lvk130_assertion> ?p ?o ?g. }
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- NP602381.RAvWo3ifV7h5GrOO40W-1h7zvj6vbBFQ94mkUqpTe3lvk130_assertion type Assertion NP602381.RAvWo3ifV7h5GrOO40W-1h7zvj6vbBFQ94mkUqpTe3lvk130_head.
- NP602381.RAvWo3ifV7h5GrOO40W-1h7zvj6vbBFQ94mkUqpTe3lvk130_assertion wasGeneratedBy ECO_0000203 NP602381.RAvWo3ifV7h5GrOO40W-1h7zvj6vbBFQ94mkUqpTe3lvk130_provenance.
- NP602381.RAvWo3ifV7h5GrOO40W-1h7zvj6vbBFQ94mkUqpTe3lvk130_assertion wasDerivedFrom befree-20150227 NP602381.RAvWo3ifV7h5GrOO40W-1h7zvj6vbBFQ94mkUqpTe3lvk130_provenance.
- NP602381.RAvWo3ifV7h5GrOO40W-1h7zvj6vbBFQ94mkUqpTe3lvk130_assertion SIO_000772 21355073 NP602381.RAvWo3ifV7h5GrOO40W-1h7zvj6vbBFQ94mkUqpTe3lvk130_provenance.
- NP602381.RAvWo3ifV7h5GrOO40W-1h7zvj6vbBFQ94mkUqpTe3lvk130_assertion evidence source_evidence_literature NP602381.RAvWo3ifV7h5GrOO40W-1h7zvj6vbBFQ94mkUqpTe3lvk130_provenance.
- NP602381.RAvWo3ifV7h5GrOO40W-1h7zvj6vbBFQ94mkUqpTe3lvk130_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." NP602381.RAvWo3ifV7h5GrOO40W-1h7zvj6vbBFQ94mkUqpTe3lvk130_provenance.