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Predicate | Object |
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rdf:type | |
calbc:hasCorrelation | |
skos:definition |
MSH: Type 2 is an autosomal dominant form with loss-of-function mutations of gene Kal2 which encodes fibroblast growth-factor receptor-1 (FGFR1 PROTEIN).
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skos:inScheme | |
skos-xl:prefLabel | |
skos-xl:altLabel |