Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP801210.RAV7NidszLAp2IlYCD5deWMxn7ifC9i8fUc1ozc50CFO8130_assertion> ?p ?o ?g. }
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- NP801210.RAV7NidszLAp2IlYCD5deWMxn7ifC9i8fUc1ozc50CFO8130_assertion type Assertion NP801210.RAV7NidszLAp2IlYCD5deWMxn7ifC9i8fUc1ozc50CFO8130_head.
- NP801210.RAV7NidszLAp2IlYCD5deWMxn7ifC9i8fUc1ozc50CFO8130_assertion description "[In addition to a new ACTA1 gene mutation, our case emphasizes the genetic heterogeneity of cap myopathy and its association with ACTA1 gene as well as the importance of repeat muscle biopsy in patients with undiagnosed muscle weakness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP801210.RAV7NidszLAp2IlYCD5deWMxn7ifC9i8fUc1ozc50CFO8130_provenance.
- NP801210.RAV7NidszLAp2IlYCD5deWMxn7ifC9i8fUc1ozc50CFO8130_assertion evidence source_evidence_literature NP801210.RAV7NidszLAp2IlYCD5deWMxn7ifC9i8fUc1ozc50CFO8130_provenance.
- NP801210.RAV7NidszLAp2IlYCD5deWMxn7ifC9i8fUc1ozc50CFO8130_assertion SIO_000772 20303757 NP801210.RAV7NidszLAp2IlYCD5deWMxn7ifC9i8fUc1ozc50CFO8130_provenance.
- NP801210.RAV7NidszLAp2IlYCD5deWMxn7ifC9i8fUc1ozc50CFO8130_assertion wasDerivedFrom befree-2016 NP801210.RAV7NidszLAp2IlYCD5deWMxn7ifC9i8fUc1ozc50CFO8130_provenance.
- NP801210.RAV7NidszLAp2IlYCD5deWMxn7ifC9i8fUc1ozc50CFO8130_assertion wasGeneratedBy ECO_0000203 NP801210.RAV7NidszLAp2IlYCD5deWMxn7ifC9i8fUc1ozc50CFO8130_provenance.