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{ ?s ?p ?o <http://purl.org/np/RAuCkR_W8_jbTlpDJ-_lzcVfyLZdHhq5l6SpN2iMEE3as#provenance>. }
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23611888
title
"
A homozygous deletion in GRID2 causes a human phenotype with cerebellar ataxia and atrophy.
"
provenance
.
assertion
SIO_000253
23611888
provenance
.