Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP512338.RAcWpShOMlv0bN-xBgF5PIHq0_eOI8zfBWYxn7HAlIotI130_assertion> ?p ?o ?g. }
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- NP512338.RAcWpShOMlv0bN-xBgF5PIHq0_eOI8zfBWYxn7HAlIotI130_assertion type Assertion NP512338.RAcWpShOMlv0bN-xBgF5PIHq0_eOI8zfBWYxn7HAlIotI130_head.
- NP512338.RAcWpShOMlv0bN-xBgF5PIHq0_eOI8zfBWYxn7HAlIotI130_assertion description "[LAMP2 mutations may account for a significant proportion of cases of HCM in children, especially when skeletal myopathy and/or WPW is present, suggesting that Danon disease is an underrecognized entity in the pediatric cardiology community.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP512338.RAcWpShOMlv0bN-xBgF5PIHq0_eOI8zfBWYxn7HAlIotI130_provenance.
- NP512338.RAcWpShOMlv0bN-xBgF5PIHq0_eOI8zfBWYxn7HAlIotI130_assertion evidence source_evidence_literature NP512338.RAcWpShOMlv0bN-xBgF5PIHq0_eOI8zfBWYxn7HAlIotI130_provenance.
- NP512338.RAcWpShOMlv0bN-xBgF5PIHq0_eOI8zfBWYxn7HAlIotI130_assertion SIO_000772 16144992 NP512338.RAcWpShOMlv0bN-xBgF5PIHq0_eOI8zfBWYxn7HAlIotI130_provenance.
- NP512338.RAcWpShOMlv0bN-xBgF5PIHq0_eOI8zfBWYxn7HAlIotI130_assertion wasDerivedFrom befree-2016 NP512338.RAcWpShOMlv0bN-xBgF5PIHq0_eOI8zfBWYxn7HAlIotI130_provenance.
- NP512338.RAcWpShOMlv0bN-xBgF5PIHq0_eOI8zfBWYxn7HAlIotI130_assertion wasGeneratedBy ECO_0000203 NP512338.RAcWpShOMlv0bN-xBgF5PIHq0_eOI8zfBWYxn7HAlIotI130_provenance.