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- NP680635.RAemqpqz9ZiFB6rSk0W2Is6iwDsqi7SL9Dn985-9hdu9M130_assertion type Assertion NP680635.RAemqpqz9ZiFB6rSk0W2Is6iwDsqi7SL9Dn985-9hdu9M130_head.
- NP680635.RAemqpqz9ZiFB6rSk0W2Is6iwDsqi7SL9Dn985-9hdu9M130_assertion wasGeneratedBy ECO_0000203 NP680635.RAemqpqz9ZiFB6rSk0W2Is6iwDsqi7SL9Dn985-9hdu9M130_provenance.
- NP680635.RAemqpqz9ZiFB6rSk0W2Is6iwDsqi7SL9Dn985-9hdu9M130_assertion wasDerivedFrom befree-20140225 NP680635.RAemqpqz9ZiFB6rSk0W2Is6iwDsqi7SL9Dn985-9hdu9M130_provenance.
- NP680635.RAemqpqz9ZiFB6rSk0W2Is6iwDsqi7SL9Dn985-9hdu9M130_assertion SIO_000772 11857753 NP680635.RAemqpqz9ZiFB6rSk0W2Is6iwDsqi7SL9Dn985-9hdu9M130_provenance.
- NP680635.RAemqpqz9ZiFB6rSk0W2Is6iwDsqi7SL9Dn985-9hdu9M130_assertion evidence source_evidence_literature NP680635.RAemqpqz9ZiFB6rSk0W2Is6iwDsqi7SL9Dn985-9hdu9M130_provenance.
- NP680635.RAemqpqz9ZiFB6rSk0W2Is6iwDsqi7SL9Dn985-9hdu9M130_assertion description "[TNNT2 gene mutations have been previously identified in individuals with a familial form of hypertrophic cardiomyopathy (FHC), an autosomal dominant inherited disease characterised by unexplained cardiac hypertrophy and high incidence of sudden death.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP680635.RAemqpqz9ZiFB6rSk0W2Is6iwDsqi7SL9Dn985-9hdu9M130_provenance.