Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[The detailed search up to December 24, 2012, identified 24 hereditary primary dystonias (DYT1 to DYT 25) that are mostly monogenic disorders, and a larger group (>70) of genetic syndromes in which dystonia is one of the characteristic clinical features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• assertion description "[The detailed search up to December 24, 2012, identified 24 hereditary primary dystonias (DYT1 to DYT 25) that are mostly monogenic disorders, and a larger group (>70) of genetic syndromes in which dystonia is one of the characteristic clinical features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[The detailed search up to December 24, 2012, identified 24 hereditary primary dystonias (DYT1 to DYT 25) that are mostly monogenic disorders, and a larger group (>70) of genetic syndromes in which dystonia is one of the characteristic clinical features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[The detailed search up to December 24, 2012, identified 24 hereditary primary dystonias (DYT1 to DYT 25) that are mostly monogenic disorders, and a larger group (>70) of genetic syndromes in which dystonia is one of the characteristic clinical features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[The detailed search up to December 24, 2012, identified 24 hereditary primary dystonias (DYT1 to DYT 25) that are mostly monogenic disorders, and a larger group (>70) of genetic syndromes in which dystonia is one of the characteristic clinical features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP362791.RAbJyeX5PhU3Urtrqw_CIaoKNAGS8vHjiI9koXHd9hCiA130_assertion description "[The detailed search up to December 24, 2012, identified 24 hereditary primary dystonias (DYT1 to DYT 25) that are mostly monogenic disorders, and a larger group (>70) of genetic syndromes in which dystonia is one of the characteristic clinical features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP362791.RAbJyeX5PhU3Urtrqw_CIaoKNAGS8vHjiI9koXHd9hCiA130_provenance.
• NP362889.RATzoDuUCvapFjSV9OaJqzvbc0ZT66Kq93Eqc6MSmQaY0130_assertion description "[The detailed search up to December 24, 2012, identified 24 hereditary primary dystonias (DYT1 to DYT 25) that are mostly monogenic disorders, and a larger group (>70) of genetic syndromes in which dystonia is one of the characteristic clinical features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP362889.RATzoDuUCvapFjSV9OaJqzvbc0ZT66Kq93Eqc6MSmQaY0130_provenance.
• NP1099055.RAeCDqtJCf_-dt1X1aQyummQeXsV3ZBSK_NWk0daCY3w8130_assertion description "[The detailed search up to December 24, 2012, identified 24 hereditary primary dystonias (DYT1 to DYT 25) that are mostly monogenic disorders, and a larger group (>70) of genetic syndromes in which dystonia is one of the characteristic clinical features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1099055.RAeCDqtJCf_-dt1X1aQyummQeXsV3ZBSK_NWk0daCY3w8130_provenance.
• NP362864.RAlxfB28OoEBDpO8B1B7oywIO_u5efAQyCfdujUwqAosc130_assertion description "[The detailed search up to December 24, 2012, identified 24 hereditary primary dystonias (DYT1 to DYT 25) that are mostly monogenic disorders, and a larger group (>70) of genetic syndromes in which dystonia is one of the characteristic clinical features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP362864.RAlxfB28OoEBDpO8B1B7oywIO_u5efAQyCfdujUwqAosc130_provenance.
• NP1099054.RAtZgMyfYOAWobkhFOX63-xQip9LZcbdzR-pUgmxh_G_g130_assertion description "[The detailed search up to December 24, 2012, identified 24 hereditary primary dystonias (DYT1 to DYT 25) that are mostly monogenic disorders, and a larger group (>70) of genetic syndromes in which dystonia is one of the characteristic clinical features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1099054.RAtZgMyfYOAWobkhFOX63-xQip9LZcbdzR-pUgmxh_G_g130_provenance.
• NP1099056.RAnl9fcVfmz1cWoqDNk2WLfeBnH3ZRiy3j_HTgQSekLsQ130_assertion description "[The detailed search up to December 24, 2012, identified 24 hereditary primary dystonias (DYT1 to DYT 25) that are mostly monogenic disorders, and a larger group (>70) of genetic syndromes in which dystonia is one of the characteristic clinical features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1099056.RAnl9fcVfmz1cWoqDNk2WLfeBnH3ZRiy3j_HTgQSekLsQ130_provenance.
• NP429420.RA_ak_GmgmA9N1qUyjs4D86kETx8RzuQ_F7MpbyP7bKpo130_assertion description "[The detailed search up to December 24, 2012, identified 24 hereditary primary dystonias (DYT1 to DYT 25) that are mostly monogenic disorders, and a larger group (>70) of genetic syndromes in which dystonia is one of the characteristic clinical features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP429420.RA_ak_GmgmA9N1qUyjs4D86kETx8RzuQ_F7MpbyP7bKpo130_provenance.
• NP429433.RA2q7BmVIIvcSTucZkDZpdyp14dPyjBXOuodPggYly3xo130_assertion description "[The detailed search up to December 24, 2012, identified 24 hereditary primary dystonias (DYT1 to DYT 25) that are mostly monogenic disorders, and a larger group (>70) of genetic syndromes in which dystonia is one of the characteristic clinical features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP429433.RA2q7BmVIIvcSTucZkDZpdyp14dPyjBXOuodPggYly3xo130_provenance.
• NP429440.RA0dq-R1yZawTDJwansmxhIHz-Uzs5hc2a8ukiviJFdto130_assertion description "[The detailed search up to December 24, 2012, identified 24 hereditary primary dystonias (DYT1 to DYT 25) that are mostly monogenic disorders, and a larger group (>70) of genetic syndromes in which dystonia is one of the characteristic clinical features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP429440.RA0dq-R1yZawTDJwansmxhIHz-Uzs5hc2a8ukiviJFdto130_provenance.
• NP1099052.RAEJ-zp2pQ-BouJRW85CBizYqbaD6vmp58HGv45lL62BI130_assertion description "[The detailed search up to December 24, 2012, identified 24 hereditary primary dystonias (DYT1 to DYT 25) that are mostly monogenic disorders, and a larger group (>70) of genetic syndromes in which dystonia is one of the characteristic clinical features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1099052.RAEJ-zp2pQ-BouJRW85CBizYqbaD6vmp58HGv45lL62BI130_provenance.
• NP1099053.RAIXIjhw_L4KMCWa5MXMLb__Y0q6zSd5DIRw5uHgL9KcY130_assertion description "[The detailed search up to December 24, 2012, identified 24 hereditary primary dystonias (DYT1 to DYT 25) that are mostly monogenic disorders, and a larger group (>70) of genetic syndromes in which dystonia is one of the characteristic clinical features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1099053.RAIXIjhw_L4KMCWa5MXMLb__Y0q6zSd5DIRw5uHgL9KcY130_provenance.
• NP1099057.RAIj2CAoTml5Bg4ArEaXG91nnHwrz5Qif-eoOrzCSmrOk130_assertion description "[The detailed search up to December 24, 2012, identified 24 hereditary primary dystonias (DYT1 to DYT 25) that are mostly monogenic disorders, and a larger group (>70) of genetic syndromes in which dystonia is one of the characteristic clinical features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1099057.RAIj2CAoTml5Bg4ArEaXG91nnHwrz5Qif-eoOrzCSmrOk130_provenance.