Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP355240.RAYsP3S6xYm3ymjaYMGkK_Rqq8E56Dzp8rLtv2UufvtPM130_assertion> ?p ?o ?g. }
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- NP355240.RAYsP3S6xYm3ymjaYMGkK_Rqq8E56Dzp8rLtv2UufvtPM130_assertion type Assertion NP355240.RAYsP3S6xYm3ymjaYMGkK_Rqq8E56Dzp8rLtv2UufvtPM130_head.
- NP355240.RAYsP3S6xYm3ymjaYMGkK_Rqq8E56Dzp8rLtv2UufvtPM130_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." NP355240.RAYsP3S6xYm3ymjaYMGkK_Rqq8E56Dzp8rLtv2UufvtPM130_provenance.
- NP355240.RAYsP3S6xYm3ymjaYMGkK_Rqq8E56Dzp8rLtv2UufvtPM130_assertion evidence source_evidence_literature NP355240.RAYsP3S6xYm3ymjaYMGkK_Rqq8E56Dzp8rLtv2UufvtPM130_provenance.
- NP355240.RAYsP3S6xYm3ymjaYMGkK_Rqq8E56Dzp8rLtv2UufvtPM130_assertion SIO_000772 17952667 NP355240.RAYsP3S6xYm3ymjaYMGkK_Rqq8E56Dzp8rLtv2UufvtPM130_provenance.
- NP355240.RAYsP3S6xYm3ymjaYMGkK_Rqq8E56Dzp8rLtv2UufvtPM130_assertion wasDerivedFrom befree-20150227 NP355240.RAYsP3S6xYm3ymjaYMGkK_Rqq8E56Dzp8rLtv2UufvtPM130_provenance.
- NP355240.RAYsP3S6xYm3ymjaYMGkK_Rqq8E56Dzp8rLtv2UufvtPM130_assertion wasGeneratedBy ECO_0000203 NP355240.RAYsP3S6xYm3ymjaYMGkK_Rqq8E56Dzp8rLtv2UufvtPM130_provenance.