Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP694357.RAjF_kmo6uWExqLb9w3aXd4BBZRCK0MBYSaQJEzc994_U130_assertion> ?p ?o ?g. }
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- NP694357.RAjF_kmo6uWExqLb9w3aXd4BBZRCK0MBYSaQJEzc994_U130_assertion type Assertion NP694357.RAjF_kmo6uWExqLb9w3aXd4BBZRCK0MBYSaQJEzc994_U130_head.
- NP694357.RAjF_kmo6uWExqLb9w3aXd4BBZRCK0MBYSaQJEzc994_U130_assertion wasGeneratedBy ECO_0000203 NP694357.RAjF_kmo6uWExqLb9w3aXd4BBZRCK0MBYSaQJEzc994_U130_provenance.
- NP694357.RAjF_kmo6uWExqLb9w3aXd4BBZRCK0MBYSaQJEzc994_U130_assertion wasDerivedFrom befree-2016 NP694357.RAjF_kmo6uWExqLb9w3aXd4BBZRCK0MBYSaQJEzc994_U130_provenance.
- NP694357.RAjF_kmo6uWExqLb9w3aXd4BBZRCK0MBYSaQJEzc994_U130_assertion SIO_000772 18808059 NP694357.RAjF_kmo6uWExqLb9w3aXd4BBZRCK0MBYSaQJEzc994_U130_provenance.
- NP694357.RAjF_kmo6uWExqLb9w3aXd4BBZRCK0MBYSaQJEzc994_U130_assertion evidence source_evidence_literature NP694357.RAjF_kmo6uWExqLb9w3aXd4BBZRCK0MBYSaQJEzc994_U130_provenance.
- NP694357.RAjF_kmo6uWExqLb9w3aXd4BBZRCK0MBYSaQJEzc994_U130_assertion description "[The homozygous or compound heterozygous mutation of the alleles of DYSF gene causes dysferlinopathy resulting in limb girdle muscular dystrophy Type 2B (LGMD 2B) or Miyoshi myopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP694357.RAjF_kmo6uWExqLb9w3aXd4BBZRCK0MBYSaQJEzc994_U130_provenance.