Matches in Nanopublications for { ?s ?p "[Achondroplasia (ACH), the most common form of human dwarfism, is caused by an activating autosomal dominant mutation in the fibroblast growth factor receptor-3 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP1260896.RASnUUld8nXbje31ETrOP_HWZCHyUV8JYrQCDbx8XS2Nc130_assertion description "[Achondroplasia (ACH), the most common form of human dwarfism, is caused by an activating autosomal dominant mutation in the fibroblast growth factor receptor-3 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1260896.RASnUUld8nXbje31ETrOP_HWZCHyUV8JYrQCDbx8XS2Nc130_provenance.