Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP512338.RAcWpShOMlv0bN-xBgF5PIHq0_eOI8zfBWYxn7HAlIotI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP512338.RAcWpShOMlv0bN-xBgF5PIHq0_eOI8zfBWYxn7HAlIotI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP512338.RAcWpShOMlv0bN-xBgF5PIHq0_eOI8zfBWYxn7HAlIotI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP512338.RAcWpShOMlv0bN-xBgF5PIHq0_eOI8zfBWYxn7HAlIotI130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP512338.RAcWpShOMlv0bN-xBgF5PIHq0_eOI8zfBWYxn7HAlIotI130_provenance.