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- NP319208.RA7zf52SNjAlmZHFR_N_1Z6nanRDa6HjHD55KwuuiuiL0130_assertion type Assertion NP319208.RA7zf52SNjAlmZHFR_N_1Z6nanRDa6HjHD55KwuuiuiL0130_head.
- NP319208.RA7zf52SNjAlmZHFR_N_1Z6nanRDa6HjHD55KwuuiuiL0130_assertion wasGeneratedBy ECO_0000203 NP319208.RA7zf52SNjAlmZHFR_N_1Z6nanRDa6HjHD55KwuuiuiL0130_provenance.
- NP319208.RA7zf52SNjAlmZHFR_N_1Z6nanRDa6HjHD55KwuuiuiL0130_assertion wasDerivedFrom befree-2016 NP319208.RA7zf52SNjAlmZHFR_N_1Z6nanRDa6HjHD55KwuuiuiL0130_provenance.
- NP319208.RA7zf52SNjAlmZHFR_N_1Z6nanRDa6HjHD55KwuuiuiL0130_assertion SIO_000772 11378820 NP319208.RA7zf52SNjAlmZHFR_N_1Z6nanRDa6HjHD55KwuuiuiL0130_provenance.
- NP319208.RA7zf52SNjAlmZHFR_N_1Z6nanRDa6HjHD55KwuuiuiL0130_assertion evidence source_evidence_literature NP319208.RA7zf52SNjAlmZHFR_N_1Z6nanRDa6HjHD55KwuuiuiL0130_provenance.
- NP319208.RA7zf52SNjAlmZHFR_N_1Z6nanRDa6HjHD55KwuuiuiL0130_assertion description "[We did not find any significant correlation between a 32-bp deletion variant of CCR5 or a single nucleotide change A1902G (Gln576Arg) of IL4RA, and IBD phenotypes, with the exception that in the UC group homozygosity for the G1902 allele of IL4RA was less frequent (0.019 vs 0.049, P=0.038).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP319208.RA7zf52SNjAlmZHFR_N_1Z6nanRDa6HjHD55KwuuiuiL0130_provenance.