Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP478861.RA5LEqW9L4rU4r3aI4QChqfxPLrDj5zCVUI9iWnlhIFU8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP478861.RA5LEqW9L4rU4r3aI4QChqfxPLrDj5zCVUI9iWnlhIFU8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP478861.RA5LEqW9L4rU4r3aI4QChqfxPLrDj5zCVUI9iWnlhIFU8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP478861.RA5LEqW9L4rU4r3aI4QChqfxPLrDj5zCVUI9iWnlhIFU8130_provenance.
- NP478861.RA5LEqW9L4rU4r3aI4QChqfxPLrDj5zCVUI9iWnlhIFU8130_assertion description "[Previously, we identified 2 functionally relevant polymorphisms in the SLC22A4 / 22A5 genes at the IBD5 locus that alter gene/protein function and comprise a 2-allele haplotype ( SLC22A -TC) associated with increased risk for Crohn's disease (CD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP478861.RA5LEqW9L4rU4r3aI4QChqfxPLrDj5zCVUI9iWnlhIFU8130_provenance.
- NP478861.RA5LEqW9L4rU4r3aI4QChqfxPLrDj5zCVUI9iWnlhIFU8130_assertion evidence source_evidence_literature NP478861.RA5LEqW9L4rU4r3aI4QChqfxPLrDj5zCVUI9iWnlhIFU8130_provenance.
- NP478861.RA5LEqW9L4rU4r3aI4QChqfxPLrDj5zCVUI9iWnlhIFU8130_assertion SIO_000772 15685536 NP478861.RA5LEqW9L4rU4r3aI4QChqfxPLrDj5zCVUI9iWnlhIFU8130_provenance.
- NP478861.RA5LEqW9L4rU4r3aI4QChqfxPLrDj5zCVUI9iWnlhIFU8130_assertion wasDerivedFrom befree-2016 NP478861.RA5LEqW9L4rU4r3aI4QChqfxPLrDj5zCVUI9iWnlhIFU8130_provenance.
- NP478861.RA5LEqW9L4rU4r3aI4QChqfxPLrDj5zCVUI9iWnlhIFU8130_assertion wasGeneratedBy ECO_0000203 NP478861.RA5LEqW9L4rU4r3aI4QChqfxPLrDj5zCVUI9iWnlhIFU8130_provenance.
- befree-2016 importedOn "2016-02-19" NP478861.RA5LEqW9L4rU4r3aI4QChqfxPLrDj5zCVUI9iWnlhIFU8130_provenance.