Matches in Nanopublications for { ?s ?p "[Mutation of RET codon 768 is associated with the FMTC phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[Mutation of RET codon 768 is associated with the FMTC phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1371037.RAlMXYsSRMccw_CabrThh5BUYOOeQ5Qg2eGrq3ItyanEk130_assertion description "[Mutation of RET codon 768 is associated with the FMTC phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1371037.RAlMXYsSRMccw_CabrThh5BUYOOeQ5Qg2eGrq3ItyanEk130_provenance.