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- NP546784.RAEJeCH8xiSqqgQni7PtTMmEGk65nSV_qThJxnhmvAxcQ130_assertion type Assertion NP546784.RAEJeCH8xiSqqgQni7PtTMmEGk65nSV_qThJxnhmvAxcQ130_head.
- NP546784.RAEJeCH8xiSqqgQni7PtTMmEGk65nSV_qThJxnhmvAxcQ130_assertion wasGeneratedBy ECO_0000203 NP546784.RAEJeCH8xiSqqgQni7PtTMmEGk65nSV_qThJxnhmvAxcQ130_provenance.
- NP546784.RAEJeCH8xiSqqgQni7PtTMmEGk65nSV_qThJxnhmvAxcQ130_assertion wasDerivedFrom befree-20140225 NP546784.RAEJeCH8xiSqqgQni7PtTMmEGk65nSV_qThJxnhmvAxcQ130_provenance.
- NP546784.RAEJeCH8xiSqqgQni7PtTMmEGk65nSV_qThJxnhmvAxcQ130_assertion SIO_000772 21355073 NP546784.RAEJeCH8xiSqqgQni7PtTMmEGk65nSV_qThJxnhmvAxcQ130_provenance.
- NP546784.RAEJeCH8xiSqqgQni7PtTMmEGk65nSV_qThJxnhmvAxcQ130_assertion evidence source_evidence_literature NP546784.RAEJeCH8xiSqqgQni7PtTMmEGk65nSV_qThJxnhmvAxcQ130_provenance.
- NP546784.RAEJeCH8xiSqqgQni7PtTMmEGk65nSV_qThJxnhmvAxcQ130_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." NP546784.RAEJeCH8xiSqqgQni7PtTMmEGk65nSV_qThJxnhmvAxcQ130_provenance.