Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP258578.RABV41lsNOQc3zEnk2E9SQw9c6tu8CBb3Bei9AKL0GmkQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP258578.RABV41lsNOQc3zEnk2E9SQw9c6tu8CBb3Bei9AKL0GmkQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP258578.RABV41lsNOQc3zEnk2E9SQw9c6tu8CBb3Bei9AKL0GmkQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP258578.RABV41lsNOQc3zEnk2E9SQw9c6tu8CBb3Bei9AKL0GmkQ130_provenance.
- NP258578.RABV41lsNOQc3zEnk2E9SQw9c6tu8CBb3Bei9AKL0GmkQ130_assertion description "[Hereditary systemic amyloidosis due to Asp76Asn variant ?2-microglobulin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP258578.RABV41lsNOQc3zEnk2E9SQw9c6tu8CBb3Bei9AKL0GmkQ130_provenance.
- NP258578.RABV41lsNOQc3zEnk2E9SQw9c6tu8CBb3Bei9AKL0GmkQ130_assertion evidence source_evidence_literature NP258578.RABV41lsNOQc3zEnk2E9SQw9c6tu8CBb3Bei9AKL0GmkQ130_provenance.
- NP258578.RABV41lsNOQc3zEnk2E9SQw9c6tu8CBb3Bei9AKL0GmkQ130_assertion SIO_000772 22693999 NP258578.RABV41lsNOQc3zEnk2E9SQw9c6tu8CBb3Bei9AKL0GmkQ130_provenance.
- NP258578.RABV41lsNOQc3zEnk2E9SQw9c6tu8CBb3Bei9AKL0GmkQ130_assertion wasDerivedFrom befree-20150227 NP258578.RABV41lsNOQc3zEnk2E9SQw9c6tu8CBb3Bei9AKL0GmkQ130_provenance.
- NP258578.RABV41lsNOQc3zEnk2E9SQw9c6tu8CBb3Bei9AKL0GmkQ130_assertion wasGeneratedBy ECO_0000203 NP258578.RABV41lsNOQc3zEnk2E9SQw9c6tu8CBb3Bei9AKL0GmkQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP258578.RABV41lsNOQc3zEnk2E9SQw9c6tu8CBb3Bei9AKL0GmkQ130_provenance.