Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP330436.RACZKnKihUmM5DePwNb9wfOCkBoWsKvzEVxdTZfN3AgW4130_assertion> ?p ?o ?g. }
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- NP330436.RACZKnKihUmM5DePwNb9wfOCkBoWsKvzEVxdTZfN3AgW4130_assertion type Assertion NP330436.RACZKnKihUmM5DePwNb9wfOCkBoWsKvzEVxdTZfN3AgW4130_head.
- NP330436.RACZKnKihUmM5DePwNb9wfOCkBoWsKvzEVxdTZfN3AgW4130_assertion wasGeneratedBy ECO_0000203 NP330436.RACZKnKihUmM5DePwNb9wfOCkBoWsKvzEVxdTZfN3AgW4130_provenance.
- NP330436.RACZKnKihUmM5DePwNb9wfOCkBoWsKvzEVxdTZfN3AgW4130_assertion wasDerivedFrom befree-2016 NP330436.RACZKnKihUmM5DePwNb9wfOCkBoWsKvzEVxdTZfN3AgW4130_provenance.
- NP330436.RACZKnKihUmM5DePwNb9wfOCkBoWsKvzEVxdTZfN3AgW4130_assertion SIO_000772 11561226 NP330436.RACZKnKihUmM5DePwNb9wfOCkBoWsKvzEVxdTZfN3AgW4130_provenance.
- NP330436.RACZKnKihUmM5DePwNb9wfOCkBoWsKvzEVxdTZfN3AgW4130_assertion evidence source_evidence_literature NP330436.RACZKnKihUmM5DePwNb9wfOCkBoWsKvzEVxdTZfN3AgW4130_provenance.
- NP330436.RACZKnKihUmM5DePwNb9wfOCkBoWsKvzEVxdTZfN3AgW4130_assertion description "[Two 4-generation white families with autosomal dominant familial dilated cardiomyopathy and conduction system disease were found to have novel mutations in the rod segment of lamin A/C.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP330436.RACZKnKihUmM5DePwNb9wfOCkBoWsKvzEVxdTZfN3AgW4130_provenance.