Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP775489.RApHMVUB6_zc89bkInPDfq0NtO4Bru3YaP1-5MVmdX3dE130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP775489.RApHMVUB6_zc89bkInPDfq0NtO4Bru3YaP1-5MVmdX3dE130_assertion type Assertion NP775489.RApHMVUB6_zc89bkInPDfq0NtO4Bru3YaP1-5MVmdX3dE130_head.
- NP775489.RApHMVUB6_zc89bkInPDfq0NtO4Bru3YaP1-5MVmdX3dE130_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." NP775489.RApHMVUB6_zc89bkInPDfq0NtO4Bru3YaP1-5MVmdX3dE130_provenance.
- NP775489.RApHMVUB6_zc89bkInPDfq0NtO4Bru3YaP1-5MVmdX3dE130_assertion evidence source_evidence_literature NP775489.RApHMVUB6_zc89bkInPDfq0NtO4Bru3YaP1-5MVmdX3dE130_provenance.
- NP775489.RApHMVUB6_zc89bkInPDfq0NtO4Bru3YaP1-5MVmdX3dE130_assertion SIO_000772 17952667 NP775489.RApHMVUB6_zc89bkInPDfq0NtO4Bru3YaP1-5MVmdX3dE130_provenance.
- NP775489.RApHMVUB6_zc89bkInPDfq0NtO4Bru3YaP1-5MVmdX3dE130_assertion wasDerivedFrom befree-20150227 NP775489.RApHMVUB6_zc89bkInPDfq0NtO4Bru3YaP1-5MVmdX3dE130_provenance.
- NP775489.RApHMVUB6_zc89bkInPDfq0NtO4Bru3YaP1-5MVmdX3dE130_assertion wasGeneratedBy ECO_0000203 NP775489.RApHMVUB6_zc89bkInPDfq0NtO4Bru3YaP1-5MVmdX3dE130_provenance.