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Mondo Disease Ontology (Rare Disease Subset)
MONDO_RARE
5031
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HNRNPA1
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http://identifiers.org/hgnc/5031
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This is just here as a test because I lose it
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Subclass of:
Thing
Related from:
has material basis in germline mutation in
amyotrophic lateral sclerosis type 20
inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 3
