Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP736078.RA25WG82KCCL7_am-ekEsbas-vmAnHMZn574Ov1QxCLFM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP736078.RA25WG82KCCL7_am-ekEsbas-vmAnHMZn574Ov1QxCLFM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP736078.RA25WG82KCCL7_am-ekEsbas-vmAnHMZn574Ov1QxCLFM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP736078.RA25WG82KCCL7_am-ekEsbas-vmAnHMZn574Ov1QxCLFM130_provenance.
- NP736078.RA25WG82KCCL7_am-ekEsbas-vmAnHMZn574Ov1QxCLFM130_assertion description "[It was 12% (3/25) in systemic lupus erythematosus, 9.5% (2/21) in primary Sj�gren's syndrome, 10% (1/10) in systemic sclerosis, 20% (2/10) in ankylosing spondylitis, 12.5% (1/8) in viral hepatitis type B, and 0% (0/2) in tuberculosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP736078.RA25WG82KCCL7_am-ekEsbas-vmAnHMZn574Ov1QxCLFM130_provenance.
- NP736078.RA25WG82KCCL7_am-ekEsbas-vmAnHMZn574Ov1QxCLFM130_assertion evidence source_evidence_literature NP736078.RA25WG82KCCL7_am-ekEsbas-vmAnHMZn574Ov1QxCLFM130_provenance.
- NP736078.RA25WG82KCCL7_am-ekEsbas-vmAnHMZn574Ov1QxCLFM130_assertion SIO_000772 19447936 NP736078.RA25WG82KCCL7_am-ekEsbas-vmAnHMZn574Ov1QxCLFM130_provenance.
- NP736078.RA25WG82KCCL7_am-ekEsbas-vmAnHMZn574Ov1QxCLFM130_assertion wasDerivedFrom befree-20140225 NP736078.RA25WG82KCCL7_am-ekEsbas-vmAnHMZn574Ov1QxCLFM130_provenance.
- NP736078.RA25WG82KCCL7_am-ekEsbas-vmAnHMZn574Ov1QxCLFM130_assertion wasGeneratedBy ECO_0000203 NP736078.RA25WG82KCCL7_am-ekEsbas-vmAnHMZn574Ov1QxCLFM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP736078.RA25WG82KCCL7_am-ekEsbas-vmAnHMZn574Ov1QxCLFM130_provenance.