Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1032191.RAvlMq5WT9GKgBJqHAKWhPHSVdILb4rzU1FErqDYlG0aM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1032191.RAvlMq5WT9GKgBJqHAKWhPHSVdILb4rzU1FErqDYlG0aM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1032191.RAvlMq5WT9GKgBJqHAKWhPHSVdILb4rzU1FErqDYlG0aM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1032191.RAvlMq5WT9GKgBJqHAKWhPHSVdILb4rzU1FErqDYlG0aM130_provenance.
- NP1032191.RAvlMq5WT9GKgBJqHAKWhPHSVdILb4rzU1FErqDYlG0aM130_assertion description "[Predominant symptom presentation in patients with hereditary TTR amyloidosis differed according to the underlying disease-causing mutation (polyneuropathy for Val30Met, cardiomyopathy for Val122Ile and Leu111Met, and mixed for Glu89Gln).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1032191.RAvlMq5WT9GKgBJqHAKWhPHSVdILb4rzU1FErqDYlG0aM130_provenance.
- NP1032191.RAvlMq5WT9GKgBJqHAKWhPHSVdILb4rzU1FErqDYlG0aM130_assertion evidence source_evidence_literature NP1032191.RAvlMq5WT9GKgBJqHAKWhPHSVdILb4rzU1FErqDYlG0aM130_provenance.
- NP1032191.RAvlMq5WT9GKgBJqHAKWhPHSVdILb4rzU1FErqDYlG0aM130_assertion SIO_000772 23193944 NP1032191.RAvlMq5WT9GKgBJqHAKWhPHSVdILb4rzU1FErqDYlG0aM130_provenance.
- NP1032191.RAvlMq5WT9GKgBJqHAKWhPHSVdILb4rzU1FErqDYlG0aM130_assertion wasDerivedFrom befree-2016 NP1032191.RAvlMq5WT9GKgBJqHAKWhPHSVdILb4rzU1FErqDYlG0aM130_provenance.
- NP1032191.RAvlMq5WT9GKgBJqHAKWhPHSVdILb4rzU1FErqDYlG0aM130_assertion wasGeneratedBy ECO_0000203 NP1032191.RAvlMq5WT9GKgBJqHAKWhPHSVdILb4rzU1FErqDYlG0aM130_provenance.
- befree-2016 importedOn "2016-02-19" NP1032191.RAvlMq5WT9GKgBJqHAKWhPHSVdILb4rzU1FErqDYlG0aM130_provenance.