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- NP417881.RAN9l7NRlM6bbOgq07bsaCRYCITeVcVTc9Ik_fNOBtWfM130_assertion type Assertion NP417881.RAN9l7NRlM6bbOgq07bsaCRYCITeVcVTc9Ik_fNOBtWfM130_head.
- NP417881.RAN9l7NRlM6bbOgq07bsaCRYCITeVcVTc9Ik_fNOBtWfM130_assertion description "[Only two patients were found with mutations in DFNB31, showing that mutations of this gene contribute to only a very small extent to USH2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP417881.RAN9l7NRlM6bbOgq07bsaCRYCITeVcVTc9Ik_fNOBtWfM130_provenance.
- NP417881.RAN9l7NRlM6bbOgq07bsaCRYCITeVcVTc9Ik_fNOBtWfM130_assertion evidence source_evidence_literature NP417881.RAN9l7NRlM6bbOgq07bsaCRYCITeVcVTc9Ik_fNOBtWfM130_provenance.
- NP417881.RAN9l7NRlM6bbOgq07bsaCRYCITeVcVTc9Ik_fNOBtWfM130_assertion SIO_000772 22147658 NP417881.RAN9l7NRlM6bbOgq07bsaCRYCITeVcVTc9Ik_fNOBtWfM130_provenance.
- NP417881.RAN9l7NRlM6bbOgq07bsaCRYCITeVcVTc9Ik_fNOBtWfM130_assertion wasDerivedFrom befree-20140225 NP417881.RAN9l7NRlM6bbOgq07bsaCRYCITeVcVTc9Ik_fNOBtWfM130_provenance.
- NP417881.RAN9l7NRlM6bbOgq07bsaCRYCITeVcVTc9Ik_fNOBtWfM130_assertion wasGeneratedBy ECO_0000203 NP417881.RAN9l7NRlM6bbOgq07bsaCRYCITeVcVTc9Ik_fNOBtWfM130_provenance.