Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1266487.RA1e0giKNoVP5o1N_J0G0xh5CYLKTLk5Q214AMxNjG7UI130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1266487.RA1e0giKNoVP5o1N_J0G0xh5CYLKTLk5Q214AMxNjG7UI130_assertion type Assertion NP1266487.RA1e0giKNoVP5o1N_J0G0xh5CYLKTLk5Q214AMxNjG7UI130_head.
- NP1266487.RA1e0giKNoVP5o1N_J0G0xh5CYLKTLk5Q214AMxNjG7UI130_assertion description "[Deletion of the PMP22 gene, results in hereditary neuropathy with liability to pressure palsies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1266487.RA1e0giKNoVP5o1N_J0G0xh5CYLKTLk5Q214AMxNjG7UI130_provenance.
- NP1266487.RA1e0giKNoVP5o1N_J0G0xh5CYLKTLk5Q214AMxNjG7UI130_assertion evidence source_evidence_literature NP1266487.RA1e0giKNoVP5o1N_J0G0xh5CYLKTLk5Q214AMxNjG7UI130_provenance.
- NP1266487.RA1e0giKNoVP5o1N_J0G0xh5CYLKTLk5Q214AMxNjG7UI130_assertion SIO_000772 25720245 NP1266487.RA1e0giKNoVP5o1N_J0G0xh5CYLKTLk5Q214AMxNjG7UI130_provenance.
- NP1266487.RA1e0giKNoVP5o1N_J0G0xh5CYLKTLk5Q214AMxNjG7UI130_assertion wasDerivedFrom befree-2016 NP1266487.RA1e0giKNoVP5o1N_J0G0xh5CYLKTLk5Q214AMxNjG7UI130_provenance.
- NP1266487.RA1e0giKNoVP5o1N_J0G0xh5CYLKTLk5Q214AMxNjG7UI130_assertion wasGeneratedBy ECO_0000203 NP1266487.RA1e0giKNoVP5o1N_J0G0xh5CYLKTLk5Q214AMxNjG7UI130_provenance.