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- source_evidence_literature type ECO_0000212 NP952194.RA4wxstcAcG0a3joF73o3AHM2pSD7GX0Z7tdQdvF-4a08130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP952194.RA4wxstcAcG0a3joF73o3AHM2pSD7GX0Z7tdQdvF-4a08130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP952194.RA4wxstcAcG0a3joF73o3AHM2pSD7GX0Z7tdQdvF-4a08130_provenance.
- NP952194.RA4wxstcAcG0a3joF73o3AHM2pSD7GX0Z7tdQdvF-4a08130_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." NP952194.RA4wxstcAcG0a3joF73o3AHM2pSD7GX0Z7tdQdvF-4a08130_provenance.
- NP952194.RA4wxstcAcG0a3joF73o3AHM2pSD7GX0Z7tdQdvF-4a08130_assertion evidence source_evidence_literature NP952194.RA4wxstcAcG0a3joF73o3AHM2pSD7GX0Z7tdQdvF-4a08130_provenance.
- NP952194.RA4wxstcAcG0a3joF73o3AHM2pSD7GX0Z7tdQdvF-4a08130_assertion SIO_000772 17875183 NP952194.RA4wxstcAcG0a3joF73o3AHM2pSD7GX0Z7tdQdvF-4a08130_provenance.
- NP952194.RA4wxstcAcG0a3joF73o3AHM2pSD7GX0Z7tdQdvF-4a08130_assertion wasDerivedFrom befree-20150227 NP952194.RA4wxstcAcG0a3joF73o3AHM2pSD7GX0Z7tdQdvF-4a08130_provenance.
- NP952194.RA4wxstcAcG0a3joF73o3AHM2pSD7GX0Z7tdQdvF-4a08130_assertion wasGeneratedBy ECO_0000203 NP952194.RA4wxstcAcG0a3joF73o3AHM2pSD7GX0Z7tdQdvF-4a08130_provenance.
- befree-20150227 importedOn "2015-02-27" NP952194.RA4wxstcAcG0a3joF73o3AHM2pSD7GX0Z7tdQdvF-4a08130_provenance.