Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP355587.RAnVJPYZD_W-u6iiaFxcJ7XqpbpPijIcCWVv1gFnsvVTg130_assertion> ?p ?o ?g. }
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- NP355587.RAnVJPYZD_W-u6iiaFxcJ7XqpbpPijIcCWVv1gFnsvVTg130_assertion type Assertion NP355587.RAnVJPYZD_W-u6iiaFxcJ7XqpbpPijIcCWVv1gFnsvVTg130_head.
- NP355587.RAnVJPYZD_W-u6iiaFxcJ7XqpbpPijIcCWVv1gFnsvVTg130_assertion description "[Deficiencies of adhalin in a particular form of limb-girdle muscular dystrophy, and of merosin in a particular form of congenital muscular dystrophy as well as the newly discovered principle of abnormal tri-nucleotide repeats in myotonic dystrophy are evidence of progress that has also amplified the notion of the dystrophinopathies that the protein-deficient muscular dystrophies can now be considered examples of contributions of the dystrophin-glycoprotein complex across the muscle fiber plasma membrane.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP355587.RAnVJPYZD_W-u6iiaFxcJ7XqpbpPijIcCWVv1gFnsvVTg130_provenance.
- NP355587.RAnVJPYZD_W-u6iiaFxcJ7XqpbpPijIcCWVv1gFnsvVTg130_assertion evidence source_evidence_literature NP355587.RAnVJPYZD_W-u6iiaFxcJ7XqpbpPijIcCWVv1gFnsvVTg130_provenance.
- NP355587.RAnVJPYZD_W-u6iiaFxcJ7XqpbpPijIcCWVv1gFnsvVTg130_assertion SIO_000772 8795845 NP355587.RAnVJPYZD_W-u6iiaFxcJ7XqpbpPijIcCWVv1gFnsvVTg130_provenance.
- NP355587.RAnVJPYZD_W-u6iiaFxcJ7XqpbpPijIcCWVv1gFnsvVTg130_assertion wasDerivedFrom befree-20150227 NP355587.RAnVJPYZD_W-u6iiaFxcJ7XqpbpPijIcCWVv1gFnsvVTg130_provenance.
- NP355587.RAnVJPYZD_W-u6iiaFxcJ7XqpbpPijIcCWVv1gFnsvVTg130_assertion wasGeneratedBy ECO_0000203 NP355587.RAnVJPYZD_W-u6iiaFxcJ7XqpbpPijIcCWVv1gFnsvVTg130_provenance.