Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP280371.RAVjqJpAd9GwJEYEZCLh1_Z_ct27qUo3bqP37McEj15Us130_assertion> ?p ?o ?g. }
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- NP280371.RAVjqJpAd9GwJEYEZCLh1_Z_ct27qUo3bqP37McEj15Us130_assertion type Assertion NP280371.RAVjqJpAd9GwJEYEZCLh1_Z_ct27qUo3bqP37McEj15Us130_head.
- NP280371.RAVjqJpAd9GwJEYEZCLh1_Z_ct27qUo3bqP37McEj15Us130_assertion description "[Limb-girdle muscular dystrophy type 2A (LGMD2A) due to mutations in the CAPN3 gene is one of the most common of autosomal recessive limb-girdle muscular dystrophies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP280371.RAVjqJpAd9GwJEYEZCLh1_Z_ct27qUo3bqP37McEj15Us130_provenance.
- NP280371.RAVjqJpAd9GwJEYEZCLh1_Z_ct27qUo3bqP37McEj15Us130_assertion evidence source_evidence_literature NP280371.RAVjqJpAd9GwJEYEZCLh1_Z_ct27qUo3bqP37McEj15Us130_provenance.
- NP280371.RAVjqJpAd9GwJEYEZCLh1_Z_ct27qUo3bqP37McEj15Us130_assertion SIO_000772 24715573 NP280371.RAVjqJpAd9GwJEYEZCLh1_Z_ct27qUo3bqP37McEj15Us130_provenance.
- NP280371.RAVjqJpAd9GwJEYEZCLh1_Z_ct27qUo3bqP37McEj15Us130_assertion wasDerivedFrom befree-20150227 NP280371.RAVjqJpAd9GwJEYEZCLh1_Z_ct27qUo3bqP37McEj15Us130_provenance.
- NP280371.RAVjqJpAd9GwJEYEZCLh1_Z_ct27qUo3bqP37McEj15Us130_assertion wasGeneratedBy ECO_0000203 NP280371.RAVjqJpAd9GwJEYEZCLh1_Z_ct27qUo3bqP37McEj15Us130_provenance.