Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP636676.RA1oNpBts9u8RQ4DaqUYmSZZ2MoOuUremF_a1yp_RJUWI130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP636676.RA1oNpBts9u8RQ4DaqUYmSZZ2MoOuUremF_a1yp_RJUWI130_assertion type Assertion NP636676.RA1oNpBts9u8RQ4DaqUYmSZZ2MoOuUremF_a1yp_RJUWI130_head.
- NP636676.RA1oNpBts9u8RQ4DaqUYmSZZ2MoOuUremF_a1yp_RJUWI130_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." NP636676.RA1oNpBts9u8RQ4DaqUYmSZZ2MoOuUremF_a1yp_RJUWI130_provenance.
- NP636676.RA1oNpBts9u8RQ4DaqUYmSZZ2MoOuUremF_a1yp_RJUWI130_assertion evidence source_evidence_literature NP636676.RA1oNpBts9u8RQ4DaqUYmSZZ2MoOuUremF_a1yp_RJUWI130_provenance.
- NP636676.RA1oNpBts9u8RQ4DaqUYmSZZ2MoOuUremF_a1yp_RJUWI130_assertion SIO_000772 17952667 NP636676.RA1oNpBts9u8RQ4DaqUYmSZZ2MoOuUremF_a1yp_RJUWI130_provenance.
- NP636676.RA1oNpBts9u8RQ4DaqUYmSZZ2MoOuUremF_a1yp_RJUWI130_assertion wasDerivedFrom befree-2016 NP636676.RA1oNpBts9u8RQ4DaqUYmSZZ2MoOuUremF_a1yp_RJUWI130_provenance.
- NP636676.RA1oNpBts9u8RQ4DaqUYmSZZ2MoOuUremF_a1yp_RJUWI130_assertion wasGeneratedBy ECO_0000203 NP636676.RA1oNpBts9u8RQ4DaqUYmSZZ2MoOuUremF_a1yp_RJUWI130_provenance.