Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP583317.RABCWBp-3ebBSxcpeQXP5gmSnmSQUTFhkQs_RCKiXQxXc130_assertion> ?p ?o ?g. }
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- NP583317.RABCWBp-3ebBSxcpeQXP5gmSnmSQUTFhkQs_RCKiXQxXc130_assertion type Assertion NP583317.RABCWBp-3ebBSxcpeQXP5gmSnmSQUTFhkQs_RCKiXQxXc130_head.
- NP583317.RABCWBp-3ebBSxcpeQXP5gmSnmSQUTFhkQs_RCKiXQxXc130_assertion description "[We previously described cross-sectional family studies of two hypertrophic cardiomyopathy (HCM)-causing mutations, R92W(TNNT2) and R403W(MYH7), both associated with minimal hypertrophy, but with widely different life expectancies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP583317.RABCWBp-3ebBSxcpeQXP5gmSnmSQUTFhkQs_RCKiXQxXc130_provenance.
- NP583317.RABCWBp-3ebBSxcpeQXP5gmSnmSQUTFhkQs_RCKiXQxXc130_assertion evidence source_evidence_literature NP583317.RABCWBp-3ebBSxcpeQXP5gmSnmSQUTFhkQs_RCKiXQxXc130_provenance.
- NP583317.RABCWBp-3ebBSxcpeQXP5gmSnmSQUTFhkQs_RCKiXQxXc130_assertion SIO_000772 17612745 NP583317.RABCWBp-3ebBSxcpeQXP5gmSnmSQUTFhkQs_RCKiXQxXc130_provenance.
- NP583317.RABCWBp-3ebBSxcpeQXP5gmSnmSQUTFhkQs_RCKiXQxXc130_assertion wasDerivedFrom befree-20150227 NP583317.RABCWBp-3ebBSxcpeQXP5gmSnmSQUTFhkQs_RCKiXQxXc130_provenance.
- NP583317.RABCWBp-3ebBSxcpeQXP5gmSnmSQUTFhkQs_RCKiXQxXc130_assertion wasGeneratedBy ECO_0000203 NP583317.RABCWBp-3ebBSxcpeQXP5gmSnmSQUTFhkQs_RCKiXQxXc130_provenance.