Matches in Nanopublications for { ?s ?p "[Mutations in ANKRD11 have recently been reported to cause KBG syndrome, an autosomal dominant condition characterized by intellectual disability (ID), behavioral problems, and macrodontia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[Mutations in ANKRD11 have recently been reported to cause KBG syndrome, an autosomal dominant condition characterized by intellectual disability (ID), behavioral problems, and macrodontia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Mutations in ANKRD11 have recently been reported to cause KBG syndrome, an autosomal dominant condition characterized by intellectual disability (ID), behavioral problems, and macrodontia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1238999.RABigq3Q_ldJIr7zdwj0c_h5h_1eIa7NH4ow241AZCF60130_assertion description "[Mutations in ANKRD11 have recently been reported to cause KBG syndrome, an autosomal dominant condition characterized by intellectual disability (ID), behavioral problems, and macrodontia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1238999.RABigq3Q_ldJIr7zdwj0c_h5h_1eIa7NH4ow241AZCF60130_provenance.
- NP1238998.RAhaEQPy8Zo0tyHv1Z1bxq-QGlC3yEzjSI-GxpwVPGuGg130_assertion description "[Mutations in ANKRD11 have recently been reported to cause KBG syndrome, an autosomal dominant condition characterized by intellectual disability (ID), behavioral problems, and macrodontia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1238998.RAhaEQPy8Zo0tyHv1Z1bxq-QGlC3yEzjSI-GxpwVPGuGg130_provenance.