Item:Q20892: Difference between revisions
Created claim: instance of (P2): rare disease (Q12388) |
Created claim: exact match (P409): http://www.orpha.net/ORDO/Orphanet_98673 |
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Property / instance of | |||
Property / instance of: class of disease / rank | |||
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Property / subclass of | |||
Property / subclass of: optic nerve disease / rank | |||
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Property / subclass of | |||
Property / subclass of: atrophy / rank | |||
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Property / subclass of | |||
Property / subclass of: disease / rank | |||
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Property / health specialty | |||
Property / health specialty: neurology / rank | |||
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Property / exact match | |||
Property / exact match: http://purl.obolibrary.org/obo/DOID_5723 / rank | |||
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Property / exact match | |||
Property / exact match: http://identifiers.org/doid/DOID:5723 / rank | |||
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Property / exact match | |||
Property / exact match: http://purl.obolibrary.org/obo/HP_0000648 / rank | |||
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Property / exact match | |||
Property / exact match: http://www.orpha.net/ORDO/Orphanet_98673 / rank | |||
Normal rank |