Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP556150.RAu-zGQxFXv4Ckn1irfpViTtDqN-9I86XJuN9VEI6xvk4130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP556150.RAu-zGQxFXv4Ckn1irfpViTtDqN-9I86XJuN9VEI6xvk4130_assertion type Assertion NP556150.RAu-zGQxFXv4Ckn1irfpViTtDqN-9I86XJuN9VEI6xvk4130_head.
- NP556150.RAu-zGQxFXv4Ckn1irfpViTtDqN-9I86XJuN9VEI6xvk4130_assertion description "[To investigate whether Leber's hereditary optic neuropathy (LHON) could be caused by mutations in OPA1 we also screened a panel of 28 LHON patients who tested negatively for the three major LHON mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP556150.RAu-zGQxFXv4Ckn1irfpViTtDqN-9I86XJuN9VEI6xvk4130_provenance.
- NP556150.RAu-zGQxFXv4Ckn1irfpViTtDqN-9I86XJuN9VEI6xvk4130_assertion evidence source_evidence_literature NP556150.RAu-zGQxFXv4Ckn1irfpViTtDqN-9I86XJuN9VEI6xvk4130_provenance.
- NP556150.RAu-zGQxFXv4Ckn1irfpViTtDqN-9I86XJuN9VEI6xvk4130_assertion SIO_000772 11440989 NP556150.RAu-zGQxFXv4Ckn1irfpViTtDqN-9I86XJuN9VEI6xvk4130_provenance.
- NP556150.RAu-zGQxFXv4Ckn1irfpViTtDqN-9I86XJuN9VEI6xvk4130_assertion wasDerivedFrom befree-20140225 NP556150.RAu-zGQxFXv4Ckn1irfpViTtDqN-9I86XJuN9VEI6xvk4130_provenance.
- NP556150.RAu-zGQxFXv4Ckn1irfpViTtDqN-9I86XJuN9VEI6xvk4130_assertion wasGeneratedBy ECO_0000203 NP556150.RAu-zGQxFXv4Ckn1irfpViTtDqN-9I86XJuN9VEI6xvk4130_provenance.