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- NP117087.RAm9sBYepC55a48pfH7Fj_jLB52VBS-OWfOmXNxwL2OzY130_assertion type Assertion NP117087.RAm9sBYepC55a48pfH7Fj_jLB52VBS-OWfOmXNxwL2OzY130_head.
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- NP117087.RAm9sBYepC55a48pfH7Fj_jLB52VBS-OWfOmXNxwL2OzY130_assertion wasDerivedFrom gad-20150221 NP117087.RAm9sBYepC55a48pfH7Fj_jLB52VBS-OWfOmXNxwL2OzY130_provenance.
- NP117087.RAm9sBYepC55a48pfH7Fj_jLB52VBS-OWfOmXNxwL2OzY130_assertion SIO_000772 17896313 NP117087.RAm9sBYepC55a48pfH7Fj_jLB52VBS-OWfOmXNxwL2OzY130_provenance.
- NP117087.RAm9sBYepC55a48pfH7Fj_jLB52VBS-OWfOmXNxwL2OzY130_assertion evidence source_evidence_literature NP117087.RAm9sBYepC55a48pfH7Fj_jLB52VBS-OWfOmXNxwL2OzY130_provenance.
- NP117087.RAm9sBYepC55a48pfH7Fj_jLB52VBS-OWfOmXNxwL2OzY130_assertion description "[Screening of the USH1G gene among Spanish patients with Usher syndrome. Lack of mutations and evidence of a minor role in the pathogenesis of the syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP117087.RAm9sBYepC55a48pfH7Fj_jLB52VBS-OWfOmXNxwL2OzY130_provenance.