Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP269471.RAROrrR3_fGwlDHHfQw60pLhOGTaMIBhLCP-LmSVzT9pE130_assertion> ?p ?o ?g. }
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- NP269471.RAROrrR3_fGwlDHHfQw60pLhOGTaMIBhLCP-LmSVzT9pE130_assertion type Assertion NP269471.RAROrrR3_fGwlDHHfQw60pLhOGTaMIBhLCP-LmSVzT9pE130_head.
- NP269471.RAROrrR3_fGwlDHHfQw60pLhOGTaMIBhLCP-LmSVzT9pE130_assertion description "[These have recently included those that encode skeletal muscle alpha-actin in autosomal dominant and autosomal recessive nemaline myopathy, nebulin and slow alpha-tropomyosin in autosomal recessive nemaline myopathy, and desmin and alpha B-crystallin in desminopathies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP269471.RAROrrR3_fGwlDHHfQw60pLhOGTaMIBhLCP-LmSVzT9pE130_provenance.
- NP269471.RAROrrR3_fGwlDHHfQw60pLhOGTaMIBhLCP-LmSVzT9pE130_assertion evidence source_evidence_literature NP269471.RAROrrR3_fGwlDHHfQw60pLhOGTaMIBhLCP-LmSVzT9pE130_provenance.
- NP269471.RAROrrR3_fGwlDHHfQw60pLhOGTaMIBhLCP-LmSVzT9pE130_assertion SIO_000772 10590887 NP269471.RAROrrR3_fGwlDHHfQw60pLhOGTaMIBhLCP-LmSVzT9pE130_provenance.
- NP269471.RAROrrR3_fGwlDHHfQw60pLhOGTaMIBhLCP-LmSVzT9pE130_assertion wasDerivedFrom befree-2016 NP269471.RAROrrR3_fGwlDHHfQw60pLhOGTaMIBhLCP-LmSVzT9pE130_provenance.
- NP269471.RAROrrR3_fGwlDHHfQw60pLhOGTaMIBhLCP-LmSVzT9pE130_assertion wasGeneratedBy ECO_0000203 NP269471.RAROrrR3_fGwlDHHfQw60pLhOGTaMIBhLCP-LmSVzT9pE130_provenance.