Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP77418.RA9RGZccbsDwbh4u-sA9MA69eE9tYqzVW4HdJK2mLJTB0130_assertion> ?p ?o ?g. }
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- NP77418.RA9RGZccbsDwbh4u-sA9MA69eE9tYqzVW4HdJK2mLJTB0130_assertion type Assertion NP77418.RA9RGZccbsDwbh4u-sA9MA69eE9tYqzVW4HdJK2mLJTB0130_head.
- NP77418.RA9RGZccbsDwbh4u-sA9MA69eE9tYqzVW4HdJK2mLJTB0130_assertion description "[We investigated disease phenotype association to genetic variations in IL23R, ATG16L1, DLG5, ABCB1/MDR1, TLR4, TNFRSF1A, chromosome 5 risk haplotype including SLC22A4 and SLC22A5, and HLA-DRB1*0103 allele among Finnish IBD patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP77418.RA9RGZccbsDwbh4u-sA9MA69eE9tYqzVW4HdJK2mLJTB0130_provenance.
- NP77418.RA9RGZccbsDwbh4u-sA9MA69eE9tYqzVW4HdJK2mLJTB0130_assertion evidence source_evidence_literature NP77418.RA9RGZccbsDwbh4u-sA9MA69eE9tYqzVW4HdJK2mLJTB0130_provenance.
- NP77418.RA9RGZccbsDwbh4u-sA9MA69eE9tYqzVW4HdJK2mLJTB0130_assertion SIO_000772 18338763 NP77418.RA9RGZccbsDwbh4u-sA9MA69eE9tYqzVW4HdJK2mLJTB0130_provenance.
- NP77418.RA9RGZccbsDwbh4u-sA9MA69eE9tYqzVW4HdJK2mLJTB0130_assertion wasDerivedFrom gad-20130706 NP77418.RA9RGZccbsDwbh4u-sA9MA69eE9tYqzVW4HdJK2mLJTB0130_provenance.
- NP77418.RA9RGZccbsDwbh4u-sA9MA69eE9tYqzVW4HdJK2mLJTB0130_assertion wasGeneratedBy ECO_0000203 NP77418.RA9RGZccbsDwbh4u-sA9MA69eE9tYqzVW4HdJK2mLJTB0130_provenance.