Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP918500.RABud5Zfn1RFTiYeMfs-KN132UYIcxLER240lEh3i7XDw130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP918500.RABud5Zfn1RFTiYeMfs-KN132UYIcxLER240lEh3i7XDw130_assertion type Assertion NP918500.RABud5Zfn1RFTiYeMfs-KN132UYIcxLER240lEh3i7XDw130_head.
- NP918500.RABud5Zfn1RFTiYeMfs-KN132UYIcxLER240lEh3i7XDw130_assertion wasGeneratedBy ECO_0000203 NP918500.RABud5Zfn1RFTiYeMfs-KN132UYIcxLER240lEh3i7XDw130_provenance.
- NP918500.RABud5Zfn1RFTiYeMfs-KN132UYIcxLER240lEh3i7XDw130_assertion wasDerivedFrom befree-20150227 NP918500.RABud5Zfn1RFTiYeMfs-KN132UYIcxLER240lEh3i7XDw130_provenance.
- NP918500.RABud5Zfn1RFTiYeMfs-KN132UYIcxLER240lEh3i7XDw130_assertion SIO_000772 22964162 NP918500.RABud5Zfn1RFTiYeMfs-KN132UYIcxLER240lEh3i7XDw130_provenance.
- NP918500.RABud5Zfn1RFTiYeMfs-KN132UYIcxLER240lEh3i7XDw130_assertion evidence source_evidence_literature NP918500.RABud5Zfn1RFTiYeMfs-KN132UYIcxLER240lEh3i7XDw130_provenance.
- NP918500.RABud5Zfn1RFTiYeMfs-KN132UYIcxLER240lEh3i7XDw130_assertion description "[An overlapping phenotypic presentation with its biological counterpart AFG3L2, which when mutated causes spinocerebellar ataxia type 28, is apparent and possibly suggests that abnormal levels of the SPG7 protein impact the function of the mitochondrial ATPases associated with diverse cellular activities-protease complex (formed by SPG7 and AFG3L2) in the cerebellum.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP918500.RABud5Zfn1RFTiYeMfs-KN132UYIcxLER240lEh3i7XDw130_provenance.