Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP502981.RAbO4tn9I--dw9AiIe_KWSAJfouKgc42cNb3J4l5DHBoc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP502981.RAbO4tn9I--dw9AiIe_KWSAJfouKgc42cNb3J4l5DHBoc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP502981.RAbO4tn9I--dw9AiIe_KWSAJfouKgc42cNb3J4l5DHBoc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP502981.RAbO4tn9I--dw9AiIe_KWSAJfouKgc42cNb3J4l5DHBoc130_provenance.
- NP502981.RAbO4tn9I--dw9AiIe_KWSAJfouKgc42cNb3J4l5DHBoc130_assertion wasGeneratedBy ECO_0000203 NP502981.RAbO4tn9I--dw9AiIe_KWSAJfouKgc42cNb3J4l5DHBoc130_provenance.
- NP502981.RAbO4tn9I--dw9AiIe_KWSAJfouKgc42cNb3J4l5DHBoc130_assertion wasDerivedFrom befree-20140225 NP502981.RAbO4tn9I--dw9AiIe_KWSAJfouKgc42cNb3J4l5DHBoc130_provenance.
- NP502981.RAbO4tn9I--dw9AiIe_KWSAJfouKgc42cNb3J4l5DHBoc130_assertion SIO_000772 11378820 NP502981.RAbO4tn9I--dw9AiIe_KWSAJfouKgc42cNb3J4l5DHBoc130_provenance.
- NP502981.RAbO4tn9I--dw9AiIe_KWSAJfouKgc42cNb3J4l5DHBoc130_assertion evidence source_evidence_literature NP502981.RAbO4tn9I--dw9AiIe_KWSAJfouKgc42cNb3J4l5DHBoc130_provenance.
- NP502981.RAbO4tn9I--dw9AiIe_KWSAJfouKgc42cNb3J4l5DHBoc130_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." NP502981.RAbO4tn9I--dw9AiIe_KWSAJfouKgc42cNb3J4l5DHBoc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP502981.RAbO4tn9I--dw9AiIe_KWSAJfouKgc42cNb3J4l5DHBoc130_provenance.