Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP107906.RAgOOGpP12sxJ1-v1YwlJNxbDhh-T9XbCsWr_HS_UiwrE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP107906.RAgOOGpP12sxJ1-v1YwlJNxbDhh-T9XbCsWr_HS_UiwrE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP107906.RAgOOGpP12sxJ1-v1YwlJNxbDhh-T9XbCsWr_HS_UiwrE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP107906.RAgOOGpP12sxJ1-v1YwlJNxbDhh-T9XbCsWr_HS_UiwrE130_provenance.
- NP107906.RAgOOGpP12sxJ1-v1YwlJNxbDhh-T9XbCsWr_HS_UiwrE130_assertion description "[Our evidence broadly supports the genetic association of OA phenotypes with an IL-1 region extended risk haplotype and specifically IL1B genotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP107906.RAgOOGpP12sxJ1-v1YwlJNxbDhh-T9XbCsWr_HS_UiwrE130_provenance.
- NP107906.RAgOOGpP12sxJ1-v1YwlJNxbDhh-T9XbCsWr_HS_UiwrE130_assertion evidence source_evidence_literature NP107906.RAgOOGpP12sxJ1-v1YwlJNxbDhh-T9XbCsWr_HS_UiwrE130_provenance.
- NP107906.RAgOOGpP12sxJ1-v1YwlJNxbDhh-T9XbCsWr_HS_UiwrE130_assertion SIO_000772 17532232 NP107906.RAgOOGpP12sxJ1-v1YwlJNxbDhh-T9XbCsWr_HS_UiwrE130_provenance.
- NP107906.RAgOOGpP12sxJ1-v1YwlJNxbDhh-T9XbCsWr_HS_UiwrE130_assertion wasDerivedFrom gad-20150221 NP107906.RAgOOGpP12sxJ1-v1YwlJNxbDhh-T9XbCsWr_HS_UiwrE130_provenance.
- NP107906.RAgOOGpP12sxJ1-v1YwlJNxbDhh-T9XbCsWr_HS_UiwrE130_assertion wasGeneratedBy ECO_0000203 NP107906.RAgOOGpP12sxJ1-v1YwlJNxbDhh-T9XbCsWr_HS_UiwrE130_provenance.
- gad-20150221 importedOn "2015-02-21" NP107906.RAgOOGpP12sxJ1-v1YwlJNxbDhh-T9XbCsWr_HS_UiwrE130_provenance.