Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1011713.RA3lfv74gbro5BMdZsUOyPJiN4645daLx8gBzR2IVR0lw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1011713.RA3lfv74gbro5BMdZsUOyPJiN4645daLx8gBzR2IVR0lw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1011713.RA3lfv74gbro5BMdZsUOyPJiN4645daLx8gBzR2IVR0lw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1011713.RA3lfv74gbro5BMdZsUOyPJiN4645daLx8gBzR2IVR0lw130_provenance.
- befree-2016 importedOn "2016-02-19" NP1011713.RA3lfv74gbro5BMdZsUOyPJiN4645daLx8gBzR2IVR0lw130_provenance.
- NP1011713.RA3lfv74gbro5BMdZsUOyPJiN4645daLx8gBzR2IVR0lw130_assertion wasGeneratedBy ECO_0000203 NP1011713.RA3lfv74gbro5BMdZsUOyPJiN4645daLx8gBzR2IVR0lw130_provenance.
- NP1011713.RA3lfv74gbro5BMdZsUOyPJiN4645daLx8gBzR2IVR0lw130_assertion wasDerivedFrom befree-2016 NP1011713.RA3lfv74gbro5BMdZsUOyPJiN4645daLx8gBzR2IVR0lw130_provenance.
- NP1011713.RA3lfv74gbro5BMdZsUOyPJiN4645daLx8gBzR2IVR0lw130_assertion SIO_000772 22964162 NP1011713.RA3lfv74gbro5BMdZsUOyPJiN4645daLx8gBzR2IVR0lw130_provenance.
- NP1011713.RA3lfv74gbro5BMdZsUOyPJiN4645daLx8gBzR2IVR0lw130_assertion evidence source_evidence_literature NP1011713.RA3lfv74gbro5BMdZsUOyPJiN4645daLx8gBzR2IVR0lw130_provenance.
- NP1011713.RA3lfv74gbro5BMdZsUOyPJiN4645daLx8gBzR2IVR0lw130_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." NP1011713.RA3lfv74gbro5BMdZsUOyPJiN4645daLx8gBzR2IVR0lw130_provenance.