Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP208607.RApKdm0Ax-Rn3gzDc-g2hjvYlX4P4G7lXrcrSOcfZQ254130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP208607.RApKdm0Ax-Rn3gzDc-g2hjvYlX4P4G7lXrcrSOcfZQ254130_assertion type Assertion NP208607.RApKdm0Ax-Rn3gzDc-g2hjvYlX4P4G7lXrcrSOcfZQ254130_head.
- NP208607.RApKdm0Ax-Rn3gzDc-g2hjvYlX4P4G7lXrcrSOcfZQ254130_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." NP208607.RApKdm0Ax-Rn3gzDc-g2hjvYlX4P4G7lXrcrSOcfZQ254130_provenance.
- NP208607.RApKdm0Ax-Rn3gzDc-g2hjvYlX4P4G7lXrcrSOcfZQ254130_assertion evidence source_evidence_literature NP208607.RApKdm0Ax-Rn3gzDc-g2hjvYlX4P4G7lXrcrSOcfZQ254130_provenance.
- NP208607.RApKdm0Ax-Rn3gzDc-g2hjvYlX4P4G7lXrcrSOcfZQ254130_assertion SIO_000772 17952667 NP208607.RApKdm0Ax-Rn3gzDc-g2hjvYlX4P4G7lXrcrSOcfZQ254130_provenance.
- NP208607.RApKdm0Ax-Rn3gzDc-g2hjvYlX4P4G7lXrcrSOcfZQ254130_assertion wasDerivedFrom befree-20140225 NP208607.RApKdm0Ax-Rn3gzDc-g2hjvYlX4P4G7lXrcrSOcfZQ254130_provenance.
- NP208607.RApKdm0Ax-Rn3gzDc-g2hjvYlX4P4G7lXrcrSOcfZQ254130_assertion wasGeneratedBy ECO_0000203 NP208607.RApKdm0Ax-Rn3gzDc-g2hjvYlX4P4G7lXrcrSOcfZQ254130_provenance.