Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP528339.RAs_ElC5YnfLiiHD6Skq8bLwHl9G6cIp5exSlZefQhtek130_assertion> ?p ?o ?g. }
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- NP528339.RAs_ElC5YnfLiiHD6Skq8bLwHl9G6cIp5exSlZefQhtek130_assertion type Assertion NP528339.RAs_ElC5YnfLiiHD6Skq8bLwHl9G6cIp5exSlZefQhtek130_head.
- NP528339.RAs_ElC5YnfLiiHD6Skq8bLwHl9G6cIp5exSlZefQhtek130_assertion description "[The protocol was standardized on a variety of known mutations, in 11 patients with cystic fibrosis (CF), Fabry's disease (FD), steroid 21-hydroxylase deficiency (21-HD) and Duchenne/Becker muscular dystrophy (DMD/BMD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP528339.RAs_ElC5YnfLiiHD6Skq8bLwHl9G6cIp5exSlZefQhtek130_provenance.
- NP528339.RAs_ElC5YnfLiiHD6Skq8bLwHl9G6cIp5exSlZefQhtek130_assertion evidence source_evidence_literature NP528339.RAs_ElC5YnfLiiHD6Skq8bLwHl9G6cIp5exSlZefQhtek130_provenance.
- NP528339.RAs_ElC5YnfLiiHD6Skq8bLwHl9G6cIp5exSlZefQhtek130_assertion SIO_000772 17952667 NP528339.RAs_ElC5YnfLiiHD6Skq8bLwHl9G6cIp5exSlZefQhtek130_provenance.
- NP528339.RAs_ElC5YnfLiiHD6Skq8bLwHl9G6cIp5exSlZefQhtek130_assertion wasDerivedFrom befree-20140225 NP528339.RAs_ElC5YnfLiiHD6Skq8bLwHl9G6cIp5exSlZefQhtek130_provenance.
- NP528339.RAs_ElC5YnfLiiHD6Skq8bLwHl9G6cIp5exSlZefQhtek130_assertion wasGeneratedBy ECO_0000203 NP528339.RAs_ElC5YnfLiiHD6Skq8bLwHl9G6cIp5exSlZefQhtek130_provenance.