Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP688474.RAiiLrx4ORBQzSi5ZUVClopSSpUb6eikErJ6iI03Teafw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP688474.RAiiLrx4ORBQzSi5ZUVClopSSpUb6eikErJ6iI03Teafw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP688474.RAiiLrx4ORBQzSi5ZUVClopSSpUb6eikErJ6iI03Teafw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP688474.RAiiLrx4ORBQzSi5ZUVClopSSpUb6eikErJ6iI03Teafw130_provenance.
- NP688474.RAiiLrx4ORBQzSi5ZUVClopSSpUb6eikErJ6iI03Teafw130_assertion description "[The haplotype with the strongest association with RA susceptibility was the FCGR3A-FCGR3B 158V-NA2 haplotype (odds ratio 3.18, 95% confidence interval 1.13-8.92 [P = 0.03] for homozygotes compared with all genotypes).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP688474.RAiiLrx4ORBQzSi5ZUVClopSSpUb6eikErJ6iI03Teafw130_provenance.
- NP688474.RAiiLrx4ORBQzSi5ZUVClopSSpUb6eikErJ6iI03Teafw130_assertion evidence source_evidence_literature NP688474.RAiiLrx4ORBQzSi5ZUVClopSSpUb6eikErJ6iI03Teafw130_provenance.
- NP688474.RAiiLrx4ORBQzSi5ZUVClopSSpUb6eikErJ6iI03Teafw130_assertion SIO_000772 16356189 NP688474.RAiiLrx4ORBQzSi5ZUVClopSSpUb6eikErJ6iI03Teafw130_provenance.
- NP688474.RAiiLrx4ORBQzSi5ZUVClopSSpUb6eikErJ6iI03Teafw130_assertion wasDerivedFrom befree-20140225 NP688474.RAiiLrx4ORBQzSi5ZUVClopSSpUb6eikErJ6iI03Teafw130_provenance.
- NP688474.RAiiLrx4ORBQzSi5ZUVClopSSpUb6eikErJ6iI03Teafw130_assertion wasGeneratedBy ECO_0000203 NP688474.RAiiLrx4ORBQzSi5ZUVClopSSpUb6eikErJ6iI03Teafw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP688474.RAiiLrx4ORBQzSi5ZUVClopSSpUb6eikErJ6iI03Teafw130_provenance.