Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP708712.RA9wcwZ1U8lqwh53aav-wI--q0pElyjXf-5_X18qTy1rM130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP708712.RA9wcwZ1U8lqwh53aav-wI--q0pElyjXf-5_X18qTy1rM130_assertion type Assertion NP708712.RA9wcwZ1U8lqwh53aav-wI--q0pElyjXf-5_X18qTy1rM130_head.
- NP708712.RA9wcwZ1U8lqwh53aav-wI--q0pElyjXf-5_X18qTy1rM130_assertion description "[After adjustment for multiple testing, we found a strong association between CLL risk and six genetic variants: CCNH (rs2266690, V270A), APAF1 (rs17028658, 3'region), IL16 (rs4505265, first intron), CASP8 (rs1045485, D302H), NOS2A (rs2779251, promoter), and CCR7 (rs3136687, intron 1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP708712.RA9wcwZ1U8lqwh53aav-wI--q0pElyjXf-5_X18qTy1rM130_provenance.
- NP708712.RA9wcwZ1U8lqwh53aav-wI--q0pElyjXf-5_X18qTy1rM130_assertion evidence source_evidence_literature NP708712.RA9wcwZ1U8lqwh53aav-wI--q0pElyjXf-5_X18qTy1rM130_provenance.
- NP708712.RA9wcwZ1U8lqwh53aav-wI--q0pElyjXf-5_X18qTy1rM130_assertion SIO_000772 19074885 NP708712.RA9wcwZ1U8lqwh53aav-wI--q0pElyjXf-5_X18qTy1rM130_provenance.
- NP708712.RA9wcwZ1U8lqwh53aav-wI--q0pElyjXf-5_X18qTy1rM130_assertion wasDerivedFrom befree-2016 NP708712.RA9wcwZ1U8lqwh53aav-wI--q0pElyjXf-5_X18qTy1rM130_provenance.
- NP708712.RA9wcwZ1U8lqwh53aav-wI--q0pElyjXf-5_X18qTy1rM130_assertion wasGeneratedBy ECO_0000203 NP708712.RA9wcwZ1U8lqwh53aav-wI--q0pElyjXf-5_X18qTy1rM130_provenance.