Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP330855.RAV_ZgY7RmlCz9H28KYeIJj1--b57Cf_D3dMUCGJvfOJQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP330855.RAV_ZgY7RmlCz9H28KYeIJj1--b57Cf_D3dMUCGJvfOJQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP330855.RAV_ZgY7RmlCz9H28KYeIJj1--b57Cf_D3dMUCGJvfOJQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP330855.RAV_ZgY7RmlCz9H28KYeIJj1--b57Cf_D3dMUCGJvfOJQ130_provenance.
- NP330855.RAV_ZgY7RmlCz9H28KYeIJj1--b57Cf_D3dMUCGJvfOJQ130_assertion description "[Mutations in troponin T (TNNT2) gene represent the important part of currently identified disease-causing mutations in hypertrophic (HCM) and dilated (DCM) cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP330855.RAV_ZgY7RmlCz9H28KYeIJj1--b57Cf_D3dMUCGJvfOJQ130_provenance.
- NP330855.RAV_ZgY7RmlCz9H28KYeIJj1--b57Cf_D3dMUCGJvfOJQ130_assertion evidence source_evidence_literature NP330855.RAV_ZgY7RmlCz9H28KYeIJj1--b57Cf_D3dMUCGJvfOJQ130_provenance.
- NP330855.RAV_ZgY7RmlCz9H28KYeIJj1--b57Cf_D3dMUCGJvfOJQ130_assertion SIO_000772 22292720 NP330855.RAV_ZgY7RmlCz9H28KYeIJj1--b57Cf_D3dMUCGJvfOJQ130_provenance.
- NP330855.RAV_ZgY7RmlCz9H28KYeIJj1--b57Cf_D3dMUCGJvfOJQ130_assertion wasDerivedFrom befree-20140225 NP330855.RAV_ZgY7RmlCz9H28KYeIJj1--b57Cf_D3dMUCGJvfOJQ130_provenance.
- NP330855.RAV_ZgY7RmlCz9H28KYeIJj1--b57Cf_D3dMUCGJvfOJQ130_assertion wasGeneratedBy ECO_0000203 NP330855.RAV_ZgY7RmlCz9H28KYeIJj1--b57Cf_D3dMUCGJvfOJQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP330855.RAV_ZgY7RmlCz9H28KYeIJj1--b57Cf_D3dMUCGJvfOJQ130_provenance.