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- NP978354.RAMr6Hmv_pWhfuCv21J8nHeMBjw57cHwvyzy_C6grNGvY130_assertion type Assertion NP978354.RAMr6Hmv_pWhfuCv21J8nHeMBjw57cHwvyzy_C6grNGvY130_head.
- NP978354.RAMr6Hmv_pWhfuCv21J8nHeMBjw57cHwvyzy_C6grNGvY130_assertion description "[This study identified, in the analyzed patient, a homozygous missense mutation in the ADAMTS18 gene, which was recently linked to Knobloch syndrome, a rare developmental disorder that affects the eye and the occipital skull.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978354.RAMr6Hmv_pWhfuCv21J8nHeMBjw57cHwvyzy_C6grNGvY130_provenance.
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- NP978354.RAMr6Hmv_pWhfuCv21J8nHeMBjw57cHwvyzy_C6grNGvY130_assertion SIO_000772 23356391 NP978354.RAMr6Hmv_pWhfuCv21J8nHeMBjw57cHwvyzy_C6grNGvY130_provenance.
- NP978354.RAMr6Hmv_pWhfuCv21J8nHeMBjw57cHwvyzy_C6grNGvY130_assertion wasDerivedFrom befree-20150227 NP978354.RAMr6Hmv_pWhfuCv21J8nHeMBjw57cHwvyzy_C6grNGvY130_provenance.
- NP978354.RAMr6Hmv_pWhfuCv21J8nHeMBjw57cHwvyzy_C6grNGvY130_assertion wasGeneratedBy ECO_0000203 NP978354.RAMr6Hmv_pWhfuCv21J8nHeMBjw57cHwvyzy_C6grNGvY130_provenance.