Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP610466.RAPf0w9qM4_8j6uDz7HqFf7lzClnCNzNljrti0KdO07qQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP610466.RAPf0w9qM4_8j6uDz7HqFf7lzClnCNzNljrti0KdO07qQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP610466.RAPf0w9qM4_8j6uDz7HqFf7lzClnCNzNljrti0KdO07qQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP610466.RAPf0w9qM4_8j6uDz7HqFf7lzClnCNzNljrti0KdO07qQ130_provenance.
- NP610466.RAPf0w9qM4_8j6uDz7HqFf7lzClnCNzNljrti0KdO07qQ130_assertion description "[At IL10, -2763A allele was found to be slightly more frequent in MG and in patients with anti-AChR than in HC group (p = 0.05, OR = 1.7, p = 0.036, OR = 1.83).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP610466.RAPf0w9qM4_8j6uDz7HqFf7lzClnCNzNljrti0KdO07qQ130_provenance.
- NP610466.RAPf0w9qM4_8j6uDz7HqFf7lzClnCNzNljrti0KdO07qQ130_assertion evidence source_evidence_literature NP610466.RAPf0w9qM4_8j6uDz7HqFf7lzClnCNzNljrti0KdO07qQ130_provenance.
- NP610466.RAPf0w9qM4_8j6uDz7HqFf7lzClnCNzNljrti0KdO07qQ130_assertion SIO_000772 17509455 NP610466.RAPf0w9qM4_8j6uDz7HqFf7lzClnCNzNljrti0KdO07qQ130_provenance.
- NP610466.RAPf0w9qM4_8j6uDz7HqFf7lzClnCNzNljrti0KdO07qQ130_assertion wasDerivedFrom befree-2016 NP610466.RAPf0w9qM4_8j6uDz7HqFf7lzClnCNzNljrti0KdO07qQ130_provenance.
- NP610466.RAPf0w9qM4_8j6uDz7HqFf7lzClnCNzNljrti0KdO07qQ130_assertion wasGeneratedBy ECO_0000203 NP610466.RAPf0w9qM4_8j6uDz7HqFf7lzClnCNzNljrti0KdO07qQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP610466.RAPf0w9qM4_8j6uDz7HqFf7lzClnCNzNljrti0KdO07qQ130_provenance.