Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP212995.RAv4ykxOUKad_L2U78jwrtmrl1wA0UJOTIzZYcwjXk8wM130_assertion> ?p ?o ?g. }
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- NP212995.RAv4ykxOUKad_L2U78jwrtmrl1wA0UJOTIzZYcwjXk8wM130_assertion type Assertion NP212995.RAv4ykxOUKad_L2U78jwrtmrl1wA0UJOTIzZYcwjXk8wM130_head.
- NP212995.RAv4ykxOUKad_L2U78jwrtmrl1wA0UJOTIzZYcwjXk8wM130_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." NP212995.RAv4ykxOUKad_L2U78jwrtmrl1wA0UJOTIzZYcwjXk8wM130_provenance.
- NP212995.RAv4ykxOUKad_L2U78jwrtmrl1wA0UJOTIzZYcwjXk8wM130_assertion evidence source_evidence_literature NP212995.RAv4ykxOUKad_L2U78jwrtmrl1wA0UJOTIzZYcwjXk8wM130_provenance.
- NP212995.RAv4ykxOUKad_L2U78jwrtmrl1wA0UJOTIzZYcwjXk8wM130_assertion SIO_000772 16144992 NP212995.RAv4ykxOUKad_L2U78jwrtmrl1wA0UJOTIzZYcwjXk8wM130_provenance.
- NP212995.RAv4ykxOUKad_L2U78jwrtmrl1wA0UJOTIzZYcwjXk8wM130_assertion wasDerivedFrom lhgdn-20090331 NP212995.RAv4ykxOUKad_L2U78jwrtmrl1wA0UJOTIzZYcwjXk8wM130_provenance.
- NP212995.RAv4ykxOUKad_L2U78jwrtmrl1wA0UJOTIzZYcwjXk8wM130_assertion wasGeneratedBy ECO_0000203 NP212995.RAv4ykxOUKad_L2U78jwrtmrl1wA0UJOTIzZYcwjXk8wM130_provenance.