Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP215547.RAf4YL1oSU5bP_-_vX-iZWh4cNB2TNGIPl-OsHFPZubtw130_assertion> ?p ?o ?g. }
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- NP215547.RAf4YL1oSU5bP_-_vX-iZWh4cNB2TNGIPl-OsHFPZubtw130_assertion type Assertion NP215547.RAf4YL1oSU5bP_-_vX-iZWh4cNB2TNGIPl-OsHFPZubtw130_head.
- NP215547.RAf4YL1oSU5bP_-_vX-iZWh4cNB2TNGIPl-OsHFPZubtw130_assertion description "[LAMP2 mutations may account for significant proportion of cases of hypertrophic cardiomyopathy children, especially when skeletal myopathy and/or Wolff-Parkinson-White syndrome is present/disease may be underrecognized in pediatric cardiology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP215547.RAf4YL1oSU5bP_-_vX-iZWh4cNB2TNGIPl-OsHFPZubtw130_provenance.
- NP215547.RAf4YL1oSU5bP_-_vX-iZWh4cNB2TNGIPl-OsHFPZubtw130_assertion evidence source_evidence_literature NP215547.RAf4YL1oSU5bP_-_vX-iZWh4cNB2TNGIPl-OsHFPZubtw130_provenance.
- NP215547.RAf4YL1oSU5bP_-_vX-iZWh4cNB2TNGIPl-OsHFPZubtw130_assertion SIO_000772 16144992 NP215547.RAf4YL1oSU5bP_-_vX-iZWh4cNB2TNGIPl-OsHFPZubtw130_provenance.
- NP215547.RAf4YL1oSU5bP_-_vX-iZWh4cNB2TNGIPl-OsHFPZubtw130_assertion wasDerivedFrom lhgdn-20090331 NP215547.RAf4YL1oSU5bP_-_vX-iZWh4cNB2TNGIPl-OsHFPZubtw130_provenance.
- NP215547.RAf4YL1oSU5bP_-_vX-iZWh4cNB2TNGIPl-OsHFPZubtw130_assertion wasGeneratedBy ECO_0000203 NP215547.RAf4YL1oSU5bP_-_vX-iZWh4cNB2TNGIPl-OsHFPZubtw130_provenance.