Item:Q22011: Difference between revisions
Created a new Item: primary bone dysplasia, human disease |
Created claim: exact match (P409): http://www.orpha.net/ORDO/Orphanet_364526 |
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| Property / instance of | |||
| Property / instance of: developmental defect during embryogenesis / rank | |||
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| Property / instance of: class of disease / rank | |||
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| Property / subclass of: rare genetic bone development disorder / rank | |||
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| Property / subclass of | |||
| Property / subclass of: rare genetic bone disease / rank | |||
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| Property / exact match | |||
| Property / exact match: http://www.orpha.net/ORDO/Orphanet_364526 / rank | |||
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