Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP690914.RAQVl8BZVihk7lNyRqnyzhu3uw1VkEcquAGHGePSIvzeU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP690914.RAQVl8BZVihk7lNyRqnyzhu3uw1VkEcquAGHGePSIvzeU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP690914.RAQVl8BZVihk7lNyRqnyzhu3uw1VkEcquAGHGePSIvzeU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP690914.RAQVl8BZVihk7lNyRqnyzhu3uw1VkEcquAGHGePSIvzeU130_provenance.
- NP690914.RAQVl8BZVihk7lNyRqnyzhu3uw1VkEcquAGHGePSIvzeU130_assertion description "[Groups of patients with rheumatoid arthritis (n = 412), systemic sclerosis (n = 224), Crohn's disease (n = 190) and healthy controls (n = 220) were genotyped for rs10889677 (exon-3'UTR C2370A), rs2201841, and rs1884444 variants; the first two have been shown to confer risk for Crohn's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP690914.RAQVl8BZVihk7lNyRqnyzhu3uw1VkEcquAGHGePSIvzeU130_provenance.
- NP690914.RAQVl8BZVihk7lNyRqnyzhu3uw1VkEcquAGHGePSIvzeU130_assertion evidence source_evidence_literature NP690914.RAQVl8BZVihk7lNyRqnyzhu3uw1VkEcquAGHGePSIvzeU130_provenance.
- NP690914.RAQVl8BZVihk7lNyRqnyzhu3uw1VkEcquAGHGePSIvzeU130_assertion SIO_000772 17606463 NP690914.RAQVl8BZVihk7lNyRqnyzhu3uw1VkEcquAGHGePSIvzeU130_provenance.
- NP690914.RAQVl8BZVihk7lNyRqnyzhu3uw1VkEcquAGHGePSIvzeU130_assertion wasDerivedFrom befree-20140225 NP690914.RAQVl8BZVihk7lNyRqnyzhu3uw1VkEcquAGHGePSIvzeU130_provenance.
- NP690914.RAQVl8BZVihk7lNyRqnyzhu3uw1VkEcquAGHGePSIvzeU130_assertion wasGeneratedBy ECO_0000203 NP690914.RAQVl8BZVihk7lNyRqnyzhu3uw1VkEcquAGHGePSIvzeU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP690914.RAQVl8BZVihk7lNyRqnyzhu3uw1VkEcquAGHGePSIvzeU130_provenance.