Matches in Nanopublications for { ?s ?p "[Mutant GTP cyclohydrolase I in autosomal dominant dystonia and recessive hyperphenylalaninemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP616496.RAerYuaH1cDgdeNFML7rwoGcce6It-Ga3figdVxPY_A2U130_assertion description "[Mutant GTP cyclohydrolase I in autosomal dominant dystonia and recessive hyperphenylalaninemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP616496.RAerYuaH1cDgdeNFML7rwoGcce6It-Ga3figdVxPY_A2U130_provenance.
- NP884436.RAu8x-J-kEMBs9QGTvDGOoREu5ebt7IVEp-HCXL4x0i7E130_assertion description "[Mutant GTP cyclohydrolase I in autosomal dominant dystonia and recessive hyperphenylalaninemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP884436.RAu8x-J-kEMBs9QGTvDGOoREu5ebt7IVEp-HCXL4x0i7E130_provenance.
- NP233843.RAjFDtTZ1BaYKj6MoWcNYUqwYcS7yNtzQ-P-DF5j0MK6U130_assertion description "[Mutant GTP cyclohydrolase I in autosomal dominant dystonia and recessive hyperphenylalaninemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP233843.RAjFDtTZ1BaYKj6MoWcNYUqwYcS7yNtzQ-P-DF5j0MK6U130_provenance.
- NP590935.RAaiI9NHDt9rVL_Go-0PGLYTlI3tXfWip7EJVqeLGnzBs130_assertion description "[Mutant GTP cyclohydrolase I in autosomal dominant dystonia and recessive hyperphenylalaninemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP590935.RAaiI9NHDt9rVL_Go-0PGLYTlI3tXfWip7EJVqeLGnzBs130_provenance.
- NP232550.RALjpErpy4-Se059BzH2Tsk9Xn7rsQL1wVhZgAEHDMuYc130_assertion description "[Mutant GTP cyclohydrolase I in autosomal dominant dystonia and recessive hyperphenylalaninemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP232550.RALjpErpy4-Se059BzH2Tsk9Xn7rsQL1wVhZgAEHDMuYc130_provenance.
- assertion description "[Mutant GTP cyclohydrolase I in autosomal dominant dystonia and recessive hyperphenylalaninemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Mutant GTP cyclohydrolase I in autosomal dominant dystonia and recessive hyperphenylalaninemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Mutant GTP cyclohydrolase I in autosomal dominant dystonia and recessive hyperphenylalaninemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP935635.RAUo29g0wRBzZrCids-gBegxslwE5tSIVwZInJ2P8poSg130_assertion description "[Mutant GTP cyclohydrolase I in autosomal dominant dystonia and recessive hyperphenylalaninemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP935635.RAUo29g0wRBzZrCids-gBegxslwE5tSIVwZInJ2P8poSg130_provenance.
- NP935648.RAXyb0VnYwHeVv-Hd7-GV9YghQivUsV8KH7IQxNyKOh-w130_assertion description "[Mutant GTP cyclohydrolase I in autosomal dominant dystonia and recessive hyperphenylalaninemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP935648.RAXyb0VnYwHeVv-Hd7-GV9YghQivUsV8KH7IQxNyKOh-w130_provenance.
- assertion description "[Mutant GTP cyclohydrolase I in autosomal dominant dystonia and recessive hyperphenylalaninemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Mutant GTP cyclohydrolase I in autosomal dominant dystonia and recessive hyperphenylalaninemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Mutant GTP cyclohydrolase I in autosomal dominant dystonia and recessive hyperphenylalaninemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1413615.RAWiGPfdtHXtYCFjpCmohVmLpUn5YMt8B__W_caan-1Jw130_assertion description "[Mutant GTP cyclohydrolase I in autosomal dominant dystonia and recessive hyperphenylalaninemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1413615.RAWiGPfdtHXtYCFjpCmohVmLpUn5YMt8B__W_caan-1Jw130_provenance.
- NP1413617.RAa8U2SLoEHD4SWd0cBK2eXX_3yaVBsgP2MxmfggggU48130_assertion description "[Mutant GTP cyclohydrolase I in autosomal dominant dystonia and recessive hyperphenylalaninemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1413617.RAa8U2SLoEHD4SWd0cBK2eXX_3yaVBsgP2MxmfggggU48130_provenance.
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- NP420630.RACb94rt3MDRxC7t0zA4yL1YZid0UpBCN6Y8L5MRYTTKo130_assertion description "[Mutant GTP cyclohydrolase I in autosomal dominant dystonia and recessive hyperphenylalaninemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP420630.RACb94rt3MDRxC7t0zA4yL1YZid0UpBCN6Y8L5MRYTTKo130_provenance.
- NP1413614.RAh5P2K78Y-jk478HFwy4SJJYzCughM7XnD6j23wl09wQ130_assertion description "[Mutant GTP cyclohydrolase I in autosomal dominant dystonia and recessive hyperphenylalaninemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1413614.RAh5P2K78Y-jk478HFwy4SJJYzCughM7XnD6j23wl09wQ130_provenance.
- NP1413616.RAreBVnenMREZ0NMx7785zoQ4rbPQlBIG6yE7JGjbtW_A130_assertion description "[Mutant GTP cyclohydrolase I in autosomal dominant dystonia and recessive hyperphenylalaninemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1413616.RAreBVnenMREZ0NMx7785zoQ4rbPQlBIG6yE7JGjbtW_A130_provenance.
- NP935620.RAPxnRAp_VVM6ymahTeysc5TPe2Dnr74f9-hKiMRvaBC4130_assertion description "[Mutant GTP cyclohydrolase I in autosomal dominant dystonia and recessive hyperphenylalaninemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP935620.RAPxnRAp_VVM6ymahTeysc5TPe2Dnr74f9-hKiMRvaBC4130_provenance.
- NP1413613.RA0sWfB08iPaZvG7afpbAP6ZAZvDqyGXT2K6kj_sWyP2A130_assertion description "[Mutant GTP cyclohydrolase I in autosomal dominant dystonia and recessive hyperphenylalaninemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1413613.RA0sWfB08iPaZvG7afpbAP6ZAZvDqyGXT2K6kj_sWyP2A130_provenance.