Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP90785.RAXraA6X8inGLYoca7bQK2O26jlPp4xznJVnFE8JXrJGQ130_assertion> ?p ?o ?g. }
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- NP90785.RAXraA6X8inGLYoca7bQK2O26jlPp4xznJVnFE8JXrJGQ130_assertion type Assertion NP90785.RAXraA6X8inGLYoca7bQK2O26jlPp4xznJVnFE8JXrJGQ130_head.
- NP90785.RAXraA6X8inGLYoca7bQK2O26jlPp4xznJVnFE8JXrJGQ130_assertion description "[Our results indicate that LGMD2A is one of the most frequent autosomal recessive disorders, thus finding its molecular characterization becoming increasingly important.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP90785.RAXraA6X8inGLYoca7bQK2O26jlPp4xznJVnFE8JXrJGQ130_provenance.
- NP90785.RAXraA6X8inGLYoca7bQK2O26jlPp4xznJVnFE8JXrJGQ130_assertion evidence source_evidence_literature NP90785.RAXraA6X8inGLYoca7bQK2O26jlPp4xznJVnFE8JXrJGQ130_provenance.
- NP90785.RAXraA6X8inGLYoca7bQK2O26jlPp4xznJVnFE8JXrJGQ130_assertion SIO_000772 15725583 NP90785.RAXraA6X8inGLYoca7bQK2O26jlPp4xznJVnFE8JXrJGQ130_provenance.
- NP90785.RAXraA6X8inGLYoca7bQK2O26jlPp4xznJVnFE8JXrJGQ130_assertion wasDerivedFrom gad-20150221 NP90785.RAXraA6X8inGLYoca7bQK2O26jlPp4xznJVnFE8JXrJGQ130_provenance.
- NP90785.RAXraA6X8inGLYoca7bQK2O26jlPp4xznJVnFE8JXrJGQ130_assertion wasGeneratedBy ECO_0000203 NP90785.RAXraA6X8inGLYoca7bQK2O26jlPp4xznJVnFE8JXrJGQ130_provenance.