Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP280387.RAvHyV_ukNFufL8kdxeciII56-b5VRLIk2GcEaAiFN8qk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP280387.RAvHyV_ukNFufL8kdxeciII56-b5VRLIk2GcEaAiFN8qk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP280387.RAvHyV_ukNFufL8kdxeciII56-b5VRLIk2GcEaAiFN8qk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP280387.RAvHyV_ukNFufL8kdxeciII56-b5VRLIk2GcEaAiFN8qk130_provenance.
- NP280387.RAvHyV_ukNFufL8kdxeciII56-b5VRLIk2GcEaAiFN8qk130_assertion description "[Secondary reduction in calpain 3 expression in patients with limb girdle muscular dystrophy type 2B and Miyoshi myopathy (primary dysferlinopathies).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP280387.RAvHyV_ukNFufL8kdxeciII56-b5VRLIk2GcEaAiFN8qk130_provenance.
- NP280387.RAvHyV_ukNFufL8kdxeciII56-b5VRLIk2GcEaAiFN8qk130_assertion evidence source_evidence_literature NP280387.RAvHyV_ukNFufL8kdxeciII56-b5VRLIk2GcEaAiFN8qk130_provenance.
- NP280387.RAvHyV_ukNFufL8kdxeciII56-b5VRLIk2GcEaAiFN8qk130_assertion SIO_000772 11053681 NP280387.RAvHyV_ukNFufL8kdxeciII56-b5VRLIk2GcEaAiFN8qk130_provenance.
- NP280387.RAvHyV_ukNFufL8kdxeciII56-b5VRLIk2GcEaAiFN8qk130_assertion wasDerivedFrom befree-20150227 NP280387.RAvHyV_ukNFufL8kdxeciII56-b5VRLIk2GcEaAiFN8qk130_provenance.
- NP280387.RAvHyV_ukNFufL8kdxeciII56-b5VRLIk2GcEaAiFN8qk130_assertion wasGeneratedBy ECO_0000203 NP280387.RAvHyV_ukNFufL8kdxeciII56-b5VRLIk2GcEaAiFN8qk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP280387.RAvHyV_ukNFufL8kdxeciII56-b5VRLIk2GcEaAiFN8qk130_provenance.