Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP416753.RAOOprKdbE5wt366pMoHYWaNL2u80DsZQLZ7aX02_4QtI130_assertion> ?p ?o ?g. }
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- NP416753.RAOOprKdbE5wt366pMoHYWaNL2u80DsZQLZ7aX02_4QtI130_assertion type Assertion NP416753.RAOOprKdbE5wt366pMoHYWaNL2u80DsZQLZ7aX02_4QtI130_head.
- NP416753.RAOOprKdbE5wt366pMoHYWaNL2u80DsZQLZ7aX02_4QtI130_assertion description "[Hypertrophic cardiomyopathy (HCM) is the most common genetic heart disease and is often a consequence of mutations in the myosin-binding protein C gene (MYBPC3).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP416753.RAOOprKdbE5wt366pMoHYWaNL2u80DsZQLZ7aX02_4QtI130_provenance.
- NP416753.RAOOprKdbE5wt366pMoHYWaNL2u80DsZQLZ7aX02_4QtI130_assertion evidence source_evidence_literature NP416753.RAOOprKdbE5wt366pMoHYWaNL2u80DsZQLZ7aX02_4QtI130_provenance.
- NP416753.RAOOprKdbE5wt366pMoHYWaNL2u80DsZQLZ7aX02_4QtI130_assertion SIO_000772 16566405 NP416753.RAOOprKdbE5wt366pMoHYWaNL2u80DsZQLZ7aX02_4QtI130_provenance.
- NP416753.RAOOprKdbE5wt366pMoHYWaNL2u80DsZQLZ7aX02_4QtI130_assertion wasDerivedFrom befree-20140225 NP416753.RAOOprKdbE5wt366pMoHYWaNL2u80DsZQLZ7aX02_4QtI130_provenance.
- NP416753.RAOOprKdbE5wt366pMoHYWaNL2u80DsZQLZ7aX02_4QtI130_assertion wasGeneratedBy ECO_0000203 NP416753.RAOOprKdbE5wt366pMoHYWaNL2u80DsZQLZ7aX02_4QtI130_provenance.