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- NP717.RADhQcHvDc7q2zYrHt8HHh7S8-iW_4fqLz14ahS0O1EPU130_assertion type Assertion NP717.RADhQcHvDc7q2zYrHt8HHh7S8-iW_4fqLz14ahS0O1EPU130_head.
- NP717.RADhQcHvDc7q2zYrHt8HHh7S8-iW_4fqLz14ahS0O1EPU130_assertion wasGeneratedBy ECO_0000218 NP717.RADhQcHvDc7q2zYrHt8HHh7S8-iW_4fqLz14ahS0O1EPU130_provenance.
- NP717.RADhQcHvDc7q2zYrHt8HHh7S8-iW_4fqLz14ahS0O1EPU130_assertion wasDerivedFrom uniprot-2016 NP717.RADhQcHvDc7q2zYrHt8HHh7S8-iW_4fqLz14ahS0O1EPU130_provenance.
- NP717.RADhQcHvDc7q2zYrHt8HHh7S8-iW_4fqLz14ahS0O1EPU130_assertion SIO_000772 10737979 NP717.RADhQcHvDc7q2zYrHt8HHh7S8-iW_4fqLz14ahS0O1EPU130_provenance.
- NP717.RADhQcHvDc7q2zYrHt8HHh7S8-iW_4fqLz14ahS0O1EPU130_assertion evidence source_evidence_curated NP717.RADhQcHvDc7q2zYrHt8HHh7S8-iW_4fqLz14ahS0O1EPU130_provenance.
- NP717.RADhQcHvDc7q2zYrHt8HHh7S8-iW_4fqLz14ahS0O1EPU130_assertion description "[Screening for mutations in the peripheral myelin genes PMP22, MPZ and Cx32 (GJB1) in Russian Charcot-Marie-Tooth neuropathy patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP717.RADhQcHvDc7q2zYrHt8HHh7S8-iW_4fqLz14ahS0O1EPU130_provenance.