Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP198139.RAa9Hgb9caSiGQx7Gs3cXSwKIqWI_hR-4k59NeCzfI0JI130_assertion> ?p ?o ?g. }
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- NP198139.RAa9Hgb9caSiGQx7Gs3cXSwKIqWI_hR-4k59NeCzfI0JI130_assertion type Assertion NP198139.RAa9Hgb9caSiGQx7Gs3cXSwKIqWI_hR-4k59NeCzfI0JI130_head.
- NP198139.RAa9Hgb9caSiGQx7Gs3cXSwKIqWI_hR-4k59NeCzfI0JI130_assertion description "[Missense mutations of ACTA1 cause an autosomal dominant congenital myopathy with cores.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP198139.RAa9Hgb9caSiGQx7Gs3cXSwKIqWI_hR-4k59NeCzfI0JI130_provenance.
- NP198139.RAa9Hgb9caSiGQx7Gs3cXSwKIqWI_hR-4k59NeCzfI0JI130_assertion evidence source_evidence_literature NP198139.RAa9Hgb9caSiGQx7Gs3cXSwKIqWI_hR-4k59NeCzfI0JI130_provenance.
- NP198139.RAa9Hgb9caSiGQx7Gs3cXSwKIqWI_hR-4k59NeCzfI0JI130_assertion SIO_000772 15520409 NP198139.RAa9Hgb9caSiGQx7Gs3cXSwKIqWI_hR-4k59NeCzfI0JI130_provenance.
- NP198139.RAa9Hgb9caSiGQx7Gs3cXSwKIqWI_hR-4k59NeCzfI0JI130_assertion wasDerivedFrom lhgdn-20090331 NP198139.RAa9Hgb9caSiGQx7Gs3cXSwKIqWI_hR-4k59NeCzfI0JI130_provenance.
- NP198139.RAa9Hgb9caSiGQx7Gs3cXSwKIqWI_hR-4k59NeCzfI0JI130_assertion wasGeneratedBy ECO_0000203 NP198139.RAa9Hgb9caSiGQx7Gs3cXSwKIqWI_hR-4k59NeCzfI0JI130_provenance.