Matches in Nanopublications for { ?s ?p "[Fragile X syndrome is a common inherited cause of mental retardation that results from loss or mutation of the fragile X mental retardation protein (FMRP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP206151.RAsRHG5QS893swzANMQRFPZNiG1_K2-dzCvpiRteomnYw130_assertion description "[Fragile X syndrome is a common inherited cause of mental retardation that results from loss or mutation of the fragile X mental retardation protein (FMRP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206151.RAsRHG5QS893swzANMQRFPZNiG1_K2-dzCvpiRteomnYw130_provenance.
- assertion description "[Fragile X syndrome is a common inherited cause of mental retardation that results from loss or mutation of the fragile X mental retardation protein (FMRP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Fragile X syndrome is a common inherited cause of mental retardation that results from loss or mutation of the fragile X mental retardation protein (FMRP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP931188.RAWGfy3kFg062t7KwTK8qB7wOOgUannnnfmOmpbleLKo0130_assertion description "[Fragile X syndrome is a common inherited cause of mental retardation that results from loss or mutation of the fragile X mental retardation protein (FMRP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP931188.RAWGfy3kFg062t7KwTK8qB7wOOgUannnnfmOmpbleLKo0130_provenance.
- NP710439.RA8p_-mfR8xzQLGgoc_dxI6LYvbLkP4xPD3evC2exZD34130_assertion description "[Fragile X syndrome is a common inherited cause of mental retardation that results from loss or mutation of the fragile X mental retardation protein (FMRP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP710439.RA8p_-mfR8xzQLGgoc_dxI6LYvbLkP4xPD3evC2exZD34130_provenance.
- NP710436.RAeVt9tWO95Q53O0r99WjKbnPA_j9H5X_uiGkvfUcDlPU130_assertion description "[Fragile X syndrome is a common inherited cause of mental retardation that results from loss or mutation of the fragile X mental retardation protein (FMRP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP710436.RAeVt9tWO95Q53O0r99WjKbnPA_j9H5X_uiGkvfUcDlPU130_provenance.
- NP710438.RAQpcdsTYgxmiRqLU_IoQwyfkWC9gd7AnBgDvqq78p2xs130_assertion description "[Fragile X syndrome is a common inherited cause of mental retardation that results from loss or mutation of the fragile X mental retardation protein (FMRP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP710438.RAQpcdsTYgxmiRqLU_IoQwyfkWC9gd7AnBgDvqq78p2xs130_provenance.
- assertion description "[Fragile X syndrome is a common inherited cause of mental retardation that results from loss or mutation of the fragile X mental retardation protein (FMRP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Fragile X syndrome is a common inherited cause of mental retardation that results from loss or mutation of the fragile X mental retardation protein (FMRP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.