Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP938095.RAXR4UJl1N1VsR0Ft6iwacAo59277mfm5Fk9ooxgbTKtM130_assertion> ?p ?o ?g. }
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- NP938095.RAXR4UJl1N1VsR0Ft6iwacAo59277mfm5Fk9ooxgbTKtM130_assertion type Assertion NP938095.RAXR4UJl1N1VsR0Ft6iwacAo59277mfm5Fk9ooxgbTKtM130_head.
- NP938095.RAXR4UJl1N1VsR0Ft6iwacAo59277mfm5Fk9ooxgbTKtM130_assertion description "[Hypertrophic cardiomyopathy (HCM) is characterized by asymmetric septal hypertrophy and is often caused by mutations in MYBPC3 gene encoding cardiac myosin-binding protein C. In contrast to humans, who are already affected at the heterozygous state, mouse models develop the phenotype mainly at the homozygous state.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP938095.RAXR4UJl1N1VsR0Ft6iwacAo59277mfm5Fk9ooxgbTKtM130_provenance.
- NP938095.RAXR4UJl1N1VsR0Ft6iwacAo59277mfm5Fk9ooxgbTKtM130_assertion evidence source_evidence_literature NP938095.RAXR4UJl1N1VsR0Ft6iwacAo59277mfm5Fk9ooxgbTKtM130_provenance.
- NP938095.RAXR4UJl1N1VsR0Ft6iwacAo59277mfm5Fk9ooxgbTKtM130_assertion SIO_000772 22076249 NP938095.RAXR4UJl1N1VsR0Ft6iwacAo59277mfm5Fk9ooxgbTKtM130_provenance.
- NP938095.RAXR4UJl1N1VsR0Ft6iwacAo59277mfm5Fk9ooxgbTKtM130_assertion wasDerivedFrom befree-2016 NP938095.RAXR4UJl1N1VsR0Ft6iwacAo59277mfm5Fk9ooxgbTKtM130_provenance.
- NP938095.RAXR4UJl1N1VsR0Ft6iwacAo59277mfm5Fk9ooxgbTKtM130_assertion wasGeneratedBy ECO_0000203 NP938095.RAXR4UJl1N1VsR0Ft6iwacAo59277mfm5Fk9ooxgbTKtM130_provenance.