Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP895248.RACFlaO7Wy7XJYA1eUU3Kr6eJXtBbqQWTGN_uo3IaWlhs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP895248.RACFlaO7Wy7XJYA1eUU3Kr6eJXtBbqQWTGN_uo3IaWlhs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP895248.RACFlaO7Wy7XJYA1eUU3Kr6eJXtBbqQWTGN_uo3IaWlhs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP895248.RACFlaO7Wy7XJYA1eUU3Kr6eJXtBbqQWTGN_uo3IaWlhs130_provenance.
- NP895248.RACFlaO7Wy7XJYA1eUU3Kr6eJXtBbqQWTGN_uo3IaWlhs130_assertion description "[Mutations of caveolin-3 cause hereditary myopathies that comprise remarkably different pathologies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP895248.RACFlaO7Wy7XJYA1eUU3Kr6eJXtBbqQWTGN_uo3IaWlhs130_provenance.
- NP895248.RACFlaO7Wy7XJYA1eUU3Kr6eJXtBbqQWTGN_uo3IaWlhs130_assertion evidence source_evidence_literature NP895248.RACFlaO7Wy7XJYA1eUU3Kr6eJXtBbqQWTGN_uo3IaWlhs130_provenance.
- NP895248.RACFlaO7Wy7XJYA1eUU3Kr6eJXtBbqQWTGN_uo3IaWlhs130_assertion SIO_000772 20472890 NP895248.RACFlaO7Wy7XJYA1eUU3Kr6eJXtBbqQWTGN_uo3IaWlhs130_provenance.
- NP895248.RACFlaO7Wy7XJYA1eUU3Kr6eJXtBbqQWTGN_uo3IaWlhs130_assertion wasDerivedFrom befree-20140225 NP895248.RACFlaO7Wy7XJYA1eUU3Kr6eJXtBbqQWTGN_uo3IaWlhs130_provenance.
- NP895248.RACFlaO7Wy7XJYA1eUU3Kr6eJXtBbqQWTGN_uo3IaWlhs130_assertion wasGeneratedBy ECO_0000203 NP895248.RACFlaO7Wy7XJYA1eUU3Kr6eJXtBbqQWTGN_uo3IaWlhs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP895248.RACFlaO7Wy7XJYA1eUU3Kr6eJXtBbqQWTGN_uo3IaWlhs130_provenance.