Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP53388.RAtst44DrMM6kM0S8V4G-iRhwkfq8FFEGU1Pi5UFtmDxc130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP53388.RAtst44DrMM6kM0S8V4G-iRhwkfq8FFEGU1Pi5UFtmDxc130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP53388.RAtst44DrMM6kM0S8V4G-iRhwkfq8FFEGU1Pi5UFtmDxc130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP53388.RAtst44DrMM6kM0S8V4G-iRhwkfq8FFEGU1Pi5UFtmDxc130_provenance.
- gwascat-2016 importedOn "2016-01-27" NP53388.RAtst44DrMM6kM0S8V4G-iRhwkfq8FFEGU1Pi5UFtmDxc130_provenance.
- NP53388.RAtst44DrMM6kM0S8V4G-iRhwkfq8FFEGU1Pi5UFtmDxc130_assertion wasGeneratedBy ECO_0000218 NP53388.RAtst44DrMM6kM0S8V4G-iRhwkfq8FFEGU1Pi5UFtmDxc130_provenance.
- NP53388.RAtst44DrMM6kM0S8V4G-iRhwkfq8FFEGU1Pi5UFtmDxc130_assertion wasDerivedFrom gwascat-2016 NP53388.RAtst44DrMM6kM0S8V4G-iRhwkfq8FFEGU1Pi5UFtmDxc130_provenance.
- NP53388.RAtst44DrMM6kM0S8V4G-iRhwkfq8FFEGU1Pi5UFtmDxc130_assertion SIO_000772 22412388 NP53388.RAtst44DrMM6kM0S8V4G-iRhwkfq8FFEGU1Pi5UFtmDxc130_provenance.
- NP53388.RAtst44DrMM6kM0S8V4G-iRhwkfq8FFEGU1Pi5UFtmDxc130_assertion evidence source_evidence_curated NP53388.RAtst44DrMM6kM0S8V4G-iRhwkfq8FFEGU1Pi5UFtmDxc130_provenance.
- NP53388.RAtst44DrMM6kM0S8V4G-iRhwkfq8FFEGU1Pi5UFtmDxc130_assertion description "[In all, the 16 replicated and newly discovered loci, in addition to the three coding NOD2 variants, accounted for 11.2% of the total genetic variance for CD risk in the AJ population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53388.RAtst44DrMM6kM0S8V4G-iRhwkfq8FFEGU1Pi5UFtmDxc130_provenance.