Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1404160.RAyPLvx61Ctxgzc2qxNwSj-4uywbyaxOC_jBtbJQcM2gg130_assertion> ?p ?o ?g. }
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- NP1404160.RAyPLvx61Ctxgzc2qxNwSj-4uywbyaxOC_jBtbJQcM2gg130_assertion type Assertion NP1404160.RAyPLvx61Ctxgzc2qxNwSj-4uywbyaxOC_jBtbJQcM2gg130_head.
- NP1404160.RAyPLvx61Ctxgzc2qxNwSj-4uywbyaxOC_jBtbJQcM2gg130_assertion description "[The results of molecular genetics studies have shown that familial hypertrophic cardiomyopathy is a disease of the sarcomere involving mutations in 7 different genes encoding proteins of the myofibrillar apparatus: ss-myosin heavy chain, ventricular myosin essential light chain, ventricular myosin regulatory light chain, cardiac troponin T, cardiac troponin I, alpha-tropomyosin, and cardiac myosin binding protein C. In addition to this locus heterogeneity, there is a wide allelic heterogeneity, since numerous mutations have been found in all these genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1404160.RAyPLvx61Ctxgzc2qxNwSj-4uywbyaxOC_jBtbJQcM2gg130_provenance.
- NP1404160.RAyPLvx61Ctxgzc2qxNwSj-4uywbyaxOC_jBtbJQcM2gg130_assertion evidence source_evidence_literature NP1404160.RAyPLvx61Ctxgzc2qxNwSj-4uywbyaxOC_jBtbJQcM2gg130_provenance.
- NP1404160.RAyPLvx61Ctxgzc2qxNwSj-4uywbyaxOC_jBtbJQcM2gg130_assertion SIO_000772 9742053 NP1404160.RAyPLvx61Ctxgzc2qxNwSj-4uywbyaxOC_jBtbJQcM2gg130_provenance.
- NP1404160.RAyPLvx61Ctxgzc2qxNwSj-4uywbyaxOC_jBtbJQcM2gg130_assertion wasDerivedFrom befree-2016 NP1404160.RAyPLvx61Ctxgzc2qxNwSj-4uywbyaxOC_jBtbJQcM2gg130_provenance.
- NP1404160.RAyPLvx61Ctxgzc2qxNwSj-4uywbyaxOC_jBtbJQcM2gg130_assertion wasGeneratedBy ECO_0000203 NP1404160.RAyPLvx61Ctxgzc2qxNwSj-4uywbyaxOC_jBtbJQcM2gg130_provenance.