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- NP776643.RAIUv-j23_9IAhcKUq43jGnqmITjLW8M5TuzKdQKhHZKk130_assertion type Assertion NP776643.RAIUv-j23_9IAhcKUq43jGnqmITjLW8M5TuzKdQKhHZKk130_head.
- NP776643.RAIUv-j23_9IAhcKUq43jGnqmITjLW8M5TuzKdQKhHZKk130_assertion wasGeneratedBy ECO_0000203 NP776643.RAIUv-j23_9IAhcKUq43jGnqmITjLW8M5TuzKdQKhHZKk130_provenance.
- NP776643.RAIUv-j23_9IAhcKUq43jGnqmITjLW8M5TuzKdQKhHZKk130_assertion wasDerivedFrom befree-20140225 NP776643.RAIUv-j23_9IAhcKUq43jGnqmITjLW8M5TuzKdQKhHZKk130_provenance.
- NP776643.RAIUv-j23_9IAhcKUq43jGnqmITjLW8M5TuzKdQKhHZKk130_assertion SIO_000772 11857753 NP776643.RAIUv-j23_9IAhcKUq43jGnqmITjLW8M5TuzKdQKhHZKk130_provenance.
- NP776643.RAIUv-j23_9IAhcKUq43jGnqmITjLW8M5TuzKdQKhHZKk130_assertion evidence source_evidence_literature NP776643.RAIUv-j23_9IAhcKUq43jGnqmITjLW8M5TuzKdQKhHZKk130_provenance.
- NP776643.RAIUv-j23_9IAhcKUq43jGnqmITjLW8M5TuzKdQKhHZKk130_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." NP776643.RAIUv-j23_9IAhcKUq43jGnqmITjLW8M5TuzKdQKhHZKk130_provenance.