Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP532275.RAQBOX9A5ctmnke7PgtahP-mUT3dF7ChTPsL9fA_lfmfQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP532275.RAQBOX9A5ctmnke7PgtahP-mUT3dF7ChTPsL9fA_lfmfQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP532275.RAQBOX9A5ctmnke7PgtahP-mUT3dF7ChTPsL9fA_lfmfQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP532275.RAQBOX9A5ctmnke7PgtahP-mUT3dF7ChTPsL9fA_lfmfQ130_provenance.
- NP532275.RAQBOX9A5ctmnke7PgtahP-mUT3dF7ChTPsL9fA_lfmfQ130_assertion description "[LAMP2 mutations may account for a significant proportion of cases of HCM in children, especially when skeletal myopathy and/or WPW is present, suggesting that Danon disease is an underrecognized entity in the pediatric cardiology community.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP532275.RAQBOX9A5ctmnke7PgtahP-mUT3dF7ChTPsL9fA_lfmfQ130_provenance.
- NP532275.RAQBOX9A5ctmnke7PgtahP-mUT3dF7ChTPsL9fA_lfmfQ130_assertion evidence source_evidence_literature NP532275.RAQBOX9A5ctmnke7PgtahP-mUT3dF7ChTPsL9fA_lfmfQ130_provenance.
- NP532275.RAQBOX9A5ctmnke7PgtahP-mUT3dF7ChTPsL9fA_lfmfQ130_assertion SIO_000772 16144992 NP532275.RAQBOX9A5ctmnke7PgtahP-mUT3dF7ChTPsL9fA_lfmfQ130_provenance.
- NP532275.RAQBOX9A5ctmnke7PgtahP-mUT3dF7ChTPsL9fA_lfmfQ130_assertion wasDerivedFrom befree-20140225 NP532275.RAQBOX9A5ctmnke7PgtahP-mUT3dF7ChTPsL9fA_lfmfQ130_provenance.
- NP532275.RAQBOX9A5ctmnke7PgtahP-mUT3dF7ChTPsL9fA_lfmfQ130_assertion wasGeneratedBy ECO_0000203 NP532275.RAQBOX9A5ctmnke7PgtahP-mUT3dF7ChTPsL9fA_lfmfQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP532275.RAQBOX9A5ctmnke7PgtahP-mUT3dF7ChTPsL9fA_lfmfQ130_provenance.