Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP232985.RAB_8pnLo5-lczVQpAAYvOCdhvcWg59z6h46kfTreg7oY130_assertion> ?p ?o ?g. }
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- NP232985.RAB_8pnLo5-lczVQpAAYvOCdhvcWg59z6h46kfTreg7oY130_assertion type Assertion NP232985.RAB_8pnLo5-lczVQpAAYvOCdhvcWg59z6h46kfTreg7oY130_head.
- NP232985.RAB_8pnLo5-lczVQpAAYvOCdhvcWg59z6h46kfTreg7oY130_assertion wasGeneratedBy ECO_0000203 NP232985.RAB_8pnLo5-lczVQpAAYvOCdhvcWg59z6h46kfTreg7oY130_provenance.
- NP232985.RAB_8pnLo5-lczVQpAAYvOCdhvcWg59z6h46kfTreg7oY130_assertion wasDerivedFrom lhgdn-20090331 NP232985.RAB_8pnLo5-lczVQpAAYvOCdhvcWg59z6h46kfTreg7oY130_provenance.
- NP232985.RAB_8pnLo5-lczVQpAAYvOCdhvcWg59z6h46kfTreg7oY130_assertion SIO_000772 18175163 NP232985.RAB_8pnLo5-lczVQpAAYvOCdhvcWg59z6h46kfTreg7oY130_provenance.
- NP232985.RAB_8pnLo5-lczVQpAAYvOCdhvcWg59z6h46kfTreg7oY130_assertion evidence source_evidence_literature NP232985.RAB_8pnLo5-lczVQpAAYvOCdhvcWg59z6h46kfTreg7oY130_provenance.
- NP232985.RAB_8pnLo5-lczVQpAAYvOCdhvcWg59z6h46kfTreg7oY130_assertion description "[the TNNI3 Pro82Ser alteration is likely a disease-modifying mutation in a severely affected individual, and, furthermore, carriers of this alteration (3% of African Americans) might be at increased risk of late-onset cardiac hypertrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP232985.RAB_8pnLo5-lczVQpAAYvOCdhvcWg59z6h46kfTreg7oY130_provenance.