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- source_evidence_literature type ECO_0000212 NP944912.RAmBJs7Kj5EkUHEA2ABlis3_NjYLmyqfrCAoV86XdNv88130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP944912.RAmBJs7Kj5EkUHEA2ABlis3_NjYLmyqfrCAoV86XdNv88130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP944912.RAmBJs7Kj5EkUHEA2ABlis3_NjYLmyqfrCAoV86XdNv88130_provenance.
- befree-2016 importedOn "2016-02-19" NP944912.RAmBJs7Kj5EkUHEA2ABlis3_NjYLmyqfrCAoV86XdNv88130_provenance.
- NP944912.RAmBJs7Kj5EkUHEA2ABlis3_NjYLmyqfrCAoV86XdNv88130_assertion wasGeneratedBy ECO_0000203 NP944912.RAmBJs7Kj5EkUHEA2ABlis3_NjYLmyqfrCAoV86XdNv88130_provenance.
- NP944912.RAmBJs7Kj5EkUHEA2ABlis3_NjYLmyqfrCAoV86XdNv88130_assertion wasDerivedFrom befree-2016 NP944912.RAmBJs7Kj5EkUHEA2ABlis3_NjYLmyqfrCAoV86XdNv88130_provenance.
- NP944912.RAmBJs7Kj5EkUHEA2ABlis3_NjYLmyqfrCAoV86XdNv88130_assertion SIO_000772 22152678 NP944912.RAmBJs7Kj5EkUHEA2ABlis3_NjYLmyqfrCAoV86XdNv88130_provenance.
- NP944912.RAmBJs7Kj5EkUHEA2ABlis3_NjYLmyqfrCAoV86XdNv88130_assertion evidence source_evidence_literature NP944912.RAmBJs7Kj5EkUHEA2ABlis3_NjYLmyqfrCAoV86XdNv88130_provenance.
- NP944912.RAmBJs7Kj5EkUHEA2ABlis3_NjYLmyqfrCAoV86XdNv88130_assertion description "[Recurrent dominant mutations affecting two adjacent residues in the motor domain of the monomeric kinesin KIF22 result in skeletal dysplasia and joint laxity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP944912.RAmBJs7Kj5EkUHEA2ABlis3_NjYLmyqfrCAoV86XdNv88130_provenance.