Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP475632.RA0P2E5T6BnB8fLoqt_UyGs2_AgUoq4__rG0y73scfe-0130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP475632.RA0P2E5T6BnB8fLoqt_UyGs2_AgUoq4__rG0y73scfe-0130_assertion type Assertion NP475632.RA0P2E5T6BnB8fLoqt_UyGs2_AgUoq4__rG0y73scfe-0130_head.
- NP475632.RA0P2E5T6BnB8fLoqt_UyGs2_AgUoq4__rG0y73scfe-0130_assertion description "[We report on novel mutations of the IDUA gene in one patient with the Scheie syndrome and in three patients with the Hurler/Scheie syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP475632.RA0P2E5T6BnB8fLoqt_UyGs2_AgUoq4__rG0y73scfe-0130_provenance.
- NP475632.RA0P2E5T6BnB8fLoqt_UyGs2_AgUoq4__rG0y73scfe-0130_assertion evidence source_evidence_literature NP475632.RA0P2E5T6BnB8fLoqt_UyGs2_AgUoq4__rG0y73scfe-0130_provenance.
- NP475632.RA0P2E5T6BnB8fLoqt_UyGs2_AgUoq4__rG0y73scfe-0130_assertion SIO_000772 7550232 NP475632.RA0P2E5T6BnB8fLoqt_UyGs2_AgUoq4__rG0y73scfe-0130_provenance.
- NP475632.RA0P2E5T6BnB8fLoqt_UyGs2_AgUoq4__rG0y73scfe-0130_assertion wasDerivedFrom befree-20150227 NP475632.RA0P2E5T6BnB8fLoqt_UyGs2_AgUoq4__rG0y73scfe-0130_provenance.
- NP475632.RA0P2E5T6BnB8fLoqt_UyGs2_AgUoq4__rG0y73scfe-0130_assertion wasGeneratedBy ECO_0000203 NP475632.RA0P2E5T6BnB8fLoqt_UyGs2_AgUoq4__rG0y73scfe-0130_provenance.