Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP814212.RAGphEmZvg73tHYgx6N16A7C8MUzRV-QM8uz3G2IT5Jm4130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP814212.RAGphEmZvg73tHYgx6N16A7C8MUzRV-QM8uz3G2IT5Jm4130_assertion type Assertion NP814212.RAGphEmZvg73tHYgx6N16A7C8MUzRV-QM8uz3G2IT5Jm4130_head.
- NP814212.RAGphEmZvg73tHYgx6N16A7C8MUzRV-QM8uz3G2IT5Jm4130_assertion description "[Mutations in the lamin A/C gene (LMNA) may cause familial dilated cardiomyopathy (dilated cardiomyopathy) characterized by early onset atrio-ventricular block (A-V block) before the manifestation of dilated cardiomyopathy and high risk of sudden death due to ventricular arrhythmia, which is very similar to the phenotype of gap junction related heart disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP814212.RAGphEmZvg73tHYgx6N16A7C8MUzRV-QM8uz3G2IT5Jm4130_provenance.
- NP814212.RAGphEmZvg73tHYgx6N16A7C8MUzRV-QM8uz3G2IT5Jm4130_assertion evidence source_evidence_literature NP814212.RAGphEmZvg73tHYgx6N16A7C8MUzRV-QM8uz3G2IT5Jm4130_provenance.
- NP814212.RAGphEmZvg73tHYgx6N16A7C8MUzRV-QM8uz3G2IT5Jm4130_assertion SIO_000772 20497714 NP814212.RAGphEmZvg73tHYgx6N16A7C8MUzRV-QM8uz3G2IT5Jm4130_provenance.
- NP814212.RAGphEmZvg73tHYgx6N16A7C8MUzRV-QM8uz3G2IT5Jm4130_assertion wasDerivedFrom befree-2016 NP814212.RAGphEmZvg73tHYgx6N16A7C8MUzRV-QM8uz3G2IT5Jm4130_provenance.
- NP814212.RAGphEmZvg73tHYgx6N16A7C8MUzRV-QM8uz3G2IT5Jm4130_assertion wasGeneratedBy ECO_0000203 NP814212.RAGphEmZvg73tHYgx6N16A7C8MUzRV-QM8uz3G2IT5Jm4130_provenance.