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- NP771465.RAOelkeZja0PVMNTdYUSZhBNj3Beyz19lhjEHFdjeQSdI130_assertion type Assertion NP771465.RAOelkeZja0PVMNTdYUSZhBNj3Beyz19lhjEHFdjeQSdI130_head.
- NP771465.RAOelkeZja0PVMNTdYUSZhBNj3Beyz19lhjEHFdjeQSdI130_assertion description "[Loss-of-function mutations in KIND1 and KIND3 cause Kindler syndrome and leukocyte adhesion deficiency-III syndrome, respectively, although no human disease has yet been associated with KIND2 gene pathology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP771465.RAOelkeZja0PVMNTdYUSZhBNj3Beyz19lhjEHFdjeQSdI130_provenance.
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- NP771465.RAOelkeZja0PVMNTdYUSZhBNj3Beyz19lhjEHFdjeQSdI130_assertion SIO_000772 19854292 NP771465.RAOelkeZja0PVMNTdYUSZhBNj3Beyz19lhjEHFdjeQSdI130_provenance.
- NP771465.RAOelkeZja0PVMNTdYUSZhBNj3Beyz19lhjEHFdjeQSdI130_assertion wasDerivedFrom befree-2016 NP771465.RAOelkeZja0PVMNTdYUSZhBNj3Beyz19lhjEHFdjeQSdI130_provenance.
- NP771465.RAOelkeZja0PVMNTdYUSZhBNj3Beyz19lhjEHFdjeQSdI130_assertion wasGeneratedBy ECO_0000203 NP771465.RAOelkeZja0PVMNTdYUSZhBNj3Beyz19lhjEHFdjeQSdI130_provenance.