Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP49848.RAQ2Gi-ZOG2niLGCmBUli6n0JQ9BHmAX2v3vgMr843Rwg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP49848.RAQ2Gi-ZOG2niLGCmBUli6n0JQ9BHmAX2v3vgMr843Rwg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP49848.RAQ2Gi-ZOG2niLGCmBUli6n0JQ9BHmAX2v3vgMr843Rwg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP49848.RAQ2Gi-ZOG2niLGCmBUli6n0JQ9BHmAX2v3vgMr843Rwg130_provenance.
- NP49848.RAQ2Gi-ZOG2niLGCmBUli6n0JQ9BHmAX2v3vgMr843Rwg130_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." NP49848.RAQ2Gi-ZOG2niLGCmBUli6n0JQ9BHmAX2v3vgMr843Rwg130_provenance.
- NP49848.RAQ2Gi-ZOG2niLGCmBUli6n0JQ9BHmAX2v3vgMr843Rwg130_assertion evidence source_evidence_literature NP49848.RAQ2Gi-ZOG2niLGCmBUli6n0JQ9BHmAX2v3vgMr843Rwg130_provenance.
- NP49848.RAQ2Gi-ZOG2niLGCmBUli6n0JQ9BHmAX2v3vgMr843Rwg130_assertion SIO_000772 18338763 NP49848.RAQ2Gi-ZOG2niLGCmBUli6n0JQ9BHmAX2v3vgMr843Rwg130_provenance.
- NP49848.RAQ2Gi-ZOG2niLGCmBUli6n0JQ9BHmAX2v3vgMr843Rwg130_assertion wasDerivedFrom gad-20130706 NP49848.RAQ2Gi-ZOG2niLGCmBUli6n0JQ9BHmAX2v3vgMr843Rwg130_provenance.
- NP49848.RAQ2Gi-ZOG2niLGCmBUli6n0JQ9BHmAX2v3vgMr843Rwg130_assertion wasGeneratedBy ECO_0000203 NP49848.RAQ2Gi-ZOG2niLGCmBUli6n0JQ9BHmAX2v3vgMr843Rwg130_provenance.
- gad-20130706 importedOn "2013-07-06" NP49848.RAQ2Gi-ZOG2niLGCmBUli6n0JQ9BHmAX2v3vgMr843Rwg130_provenance.