Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP281282.RAckKXFiiICyilM9D_4DOnGk8XqeNnjNkcHBaLtEeKh-k130_assertion> ?p ?o ?g. }
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- NP281282.RAckKXFiiICyilM9D_4DOnGk8XqeNnjNkcHBaLtEeKh-k130_assertion type Assertion NP281282.RAckKXFiiICyilM9D_4DOnGk8XqeNnjNkcHBaLtEeKh-k130_head.
- NP281282.RAckKXFiiICyilM9D_4DOnGk8XqeNnjNkcHBaLtEeKh-k130_assertion wasGeneratedBy ECO_0000203 NP281282.RAckKXFiiICyilM9D_4DOnGk8XqeNnjNkcHBaLtEeKh-k130_provenance.
- NP281282.RAckKXFiiICyilM9D_4DOnGk8XqeNnjNkcHBaLtEeKh-k130_assertion wasDerivedFrom befree-20140225 NP281282.RAckKXFiiICyilM9D_4DOnGk8XqeNnjNkcHBaLtEeKh-k130_provenance.
- NP281282.RAckKXFiiICyilM9D_4DOnGk8XqeNnjNkcHBaLtEeKh-k130_assertion SIO_000772 11561226 NP281282.RAckKXFiiICyilM9D_4DOnGk8XqeNnjNkcHBaLtEeKh-k130_provenance.
- NP281282.RAckKXFiiICyilM9D_4DOnGk8XqeNnjNkcHBaLtEeKh-k130_assertion evidence source_evidence_literature NP281282.RAckKXFiiICyilM9D_4DOnGk8XqeNnjNkcHBaLtEeKh-k130_provenance.
- NP281282.RAckKXFiiICyilM9D_4DOnGk8XqeNnjNkcHBaLtEeKh-k130_assertion description "[Novel rod segment mutations in lamin A/C cause variable conduction system disease and dilated cardiomyopathy without skeletal myopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281282.RAckKXFiiICyilM9D_4DOnGk8XqeNnjNkcHBaLtEeKh-k130_provenance.