Matches in Nanopublications for { ?s ?p "[The G380R mutation in the transmembrane domain of fibroblast growth factor receptor 3 (FGFR3) causes achondroplasia, the most common form of human dwarfism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[The G380R mutation in the transmembrane domain of fibroblast growth factor receptor 3 (FGFR3) causes achondroplasia, the most common form of human dwarfism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP400916.RAZMeJNI4OOlDTktQeIwUuL40lS7_eUIB9kQzxxDjMpJ0130_assertion description "[The G380R mutation in the transmembrane domain of fibroblast growth factor receptor 3 (FGFR3) causes achondroplasia, the most common form of human dwarfism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP400916.RAZMeJNI4OOlDTktQeIwUuL40lS7_eUIB9kQzxxDjMpJ0130_provenance.
- NP872656.RAyCgqjQ6DyVGlCEXieR6HozXI5OPtTDztWdYXl_uQObs130_assertion description "[The G380R mutation in the transmembrane domain of fibroblast growth factor receptor 3 (FGFR3) causes achondroplasia, the most common form of human dwarfism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP872656.RAyCgqjQ6DyVGlCEXieR6HozXI5OPtTDztWdYXl_uQObs130_provenance.