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- NP875482.RAp8N9F2i8c_7Vl0eZ0TBVpNnjRcUw-djU5xcrJ3VTm70130_assertion type Assertion NP875482.RAp8N9F2i8c_7Vl0eZ0TBVpNnjRcUw-djU5xcrJ3VTm70130_head.
- NP875482.RAp8N9F2i8c_7Vl0eZ0TBVpNnjRcUw-djU5xcrJ3VTm70130_assertion wasGeneratedBy ECO_0000203 NP875482.RAp8N9F2i8c_7Vl0eZ0TBVpNnjRcUw-djU5xcrJ3VTm70130_provenance.
- NP875482.RAp8N9F2i8c_7Vl0eZ0TBVpNnjRcUw-djU5xcrJ3VTm70130_assertion wasDerivedFrom befree-2016 NP875482.RAp8N9F2i8c_7Vl0eZ0TBVpNnjRcUw-djU5xcrJ3VTm70130_provenance.
- NP875482.RAp8N9F2i8c_7Vl0eZ0TBVpNnjRcUw-djU5xcrJ3VTm70130_assertion SIO_000772 21355073 NP875482.RAp8N9F2i8c_7Vl0eZ0TBVpNnjRcUw-djU5xcrJ3VTm70130_provenance.
- NP875482.RAp8N9F2i8c_7Vl0eZ0TBVpNnjRcUw-djU5xcrJ3VTm70130_assertion evidence source_evidence_literature NP875482.RAp8N9F2i8c_7Vl0eZ0TBVpNnjRcUw-djU5xcrJ3VTm70130_provenance.
- NP875482.RAp8N9F2i8c_7Vl0eZ0TBVpNnjRcUw-djU5xcrJ3VTm70130_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." NP875482.RAp8N9F2i8c_7Vl0eZ0TBVpNnjRcUw-djU5xcrJ3VTm70130_provenance.