Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP86358.RAfG5MnqPbRNIRS5aT_R1z8wW-vZWi5zGslsh883MK2i0130_assertion> ?p ?o ?g. }
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- NP86358.RAfG5MnqPbRNIRS5aT_R1z8wW-vZWi5zGslsh883MK2i0130_assertion type Assertion NP86358.RAfG5MnqPbRNIRS5aT_R1z8wW-vZWi5zGslsh883MK2i0130_head.
- NP86358.RAfG5MnqPbRNIRS5aT_R1z8wW-vZWi5zGslsh883MK2i0130_assertion description "[Our data associated the R349L and R190W mutations in LMNA with severe forms of familial DC. LMNA mutations should be considered in the genetic screening of patients with familial DC without conduction system disease. Isolated left ventricular noncompactio]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP86358.RAfG5MnqPbRNIRS5aT_R1z8wW-vZWi5zGslsh883MK2i0130_provenance.
- NP86358.RAfG5MnqPbRNIRS5aT_R1z8wW-vZWi5zGslsh883MK2i0130_assertion evidence source_evidence_literature NP86358.RAfG5MnqPbRNIRS5aT_R1z8wW-vZWi5zGslsh883MK2i0130_provenance.
- NP86358.RAfG5MnqPbRNIRS5aT_R1z8wW-vZWi5zGslsh883MK2i0130_assertion SIO_000772 15219508 NP86358.RAfG5MnqPbRNIRS5aT_R1z8wW-vZWi5zGslsh883MK2i0130_provenance.
- NP86358.RAfG5MnqPbRNIRS5aT_R1z8wW-vZWi5zGslsh883MK2i0130_assertion wasDerivedFrom gad-20150221 NP86358.RAfG5MnqPbRNIRS5aT_R1z8wW-vZWi5zGslsh883MK2i0130_provenance.
- NP86358.RAfG5MnqPbRNIRS5aT_R1z8wW-vZWi5zGslsh883MK2i0130_assertion wasGeneratedBy ECO_0000203 NP86358.RAfG5MnqPbRNIRS5aT_R1z8wW-vZWi5zGslsh883MK2i0130_provenance.