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[The combined analysis identified new, significant associations with CRC at 1p36.2 marked by rs72647484 (minor allele frequency [MAF]?=?0.09) near CDC42 and WNT4 (P?=?1.21?�?10(-8), odds ratio [OR]?=?1.21 ) and at 16q24.1 marked by rs16941835 (MAF?=?0.21, P?=?5.06?�?10(-8); OR?=?1.15) within the long non-coding RNA (lncRNA) RP11-58A18.1 and ~500?kb from the nearest coding gene FOXL1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
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Gene-disease associations inferred from text-mining the literature.
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DisGeNET evidence - LITERATURE
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