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- source_evidence_literature type ECO_0000212 NP630359.RAe98_U8jNmk4X3QXlT6FiGyd7o4yaETQIm1l1bbTvAOk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP630359.RAe98_U8jNmk4X3QXlT6FiGyd7o4yaETQIm1l1bbTvAOk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP630359.RAe98_U8jNmk4X3QXlT6FiGyd7o4yaETQIm1l1bbTvAOk130_provenance.
- NP630359.RAe98_U8jNmk4X3QXlT6FiGyd7o4yaETQIm1l1bbTvAOk130_assertion description "[MBL2 structural gene polymorphisms at codon 52 (CGT-->TGT, Arg-->Cys; D), codon 54 (GGC-->GAC, Gly-->Asp; B) and codon 57 (GGA-->GAA, Gly--> Glu; C), and MBL2 promoter region polymorphism at position -221 (G-->C) were examined in 57 patients with RA complicated by biopsy-proven reactive amyloidosis and 51 control RA patients without amyloid.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP630359.RAe98_U8jNmk4X3QXlT6FiGyd7o4yaETQIm1l1bbTvAOk130_provenance.
- NP630359.RAe98_U8jNmk4X3QXlT6FiGyd7o4yaETQIm1l1bbTvAOk130_assertion evidence source_evidence_literature NP630359.RAe98_U8jNmk4X3QXlT6FiGyd7o4yaETQIm1l1bbTvAOk130_provenance.
- NP630359.RAe98_U8jNmk4X3QXlT6FiGyd7o4yaETQIm1l1bbTvAOk130_assertion SIO_000772 17875183 NP630359.RAe98_U8jNmk4X3QXlT6FiGyd7o4yaETQIm1l1bbTvAOk130_provenance.
- NP630359.RAe98_U8jNmk4X3QXlT6FiGyd7o4yaETQIm1l1bbTvAOk130_assertion wasDerivedFrom befree-2016 NP630359.RAe98_U8jNmk4X3QXlT6FiGyd7o4yaETQIm1l1bbTvAOk130_provenance.
- NP630359.RAe98_U8jNmk4X3QXlT6FiGyd7o4yaETQIm1l1bbTvAOk130_assertion wasGeneratedBy ECO_0000203 NP630359.RAe98_U8jNmk4X3QXlT6FiGyd7o4yaETQIm1l1bbTvAOk130_provenance.
- befree-2016 importedOn "2016-02-19" NP630359.RAe98_U8jNmk4X3QXlT6FiGyd7o4yaETQIm1l1bbTvAOk130_provenance.