Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[The disease gene has been identified in 10 primary dystonias, seven autosomal dominant (TOR1A/DYT1, GCH1/DYT5a, THAP1/DYT6, PNKD1/MR-1/DYT8, SGCE/DYT11, ATP1A3/DYT12 and SLC2A1/DYT18), two autosomal recessive (TH/DYT5b and PRKRA/DYT16) and one X-chromosomal recessive (TAF1/DYT3).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP735454.RAd62_jeyWn1GIbMHAtuExk2-ZO_gMcvMQMEnsWi9Xmm0130_assertion description "[The disease gene has been identified in 10 primary dystonias, seven autosomal dominant (TOR1A/DYT1, GCH1/DYT5a, THAP1/DYT6, PNKD1/MR-1/DYT8, SGCE/DYT11, ATP1A3/DYT12 and SLC2A1/DYT18), two autosomal recessive (TH/DYT5b and PRKRA/DYT16) and one X-chromosomal recessive (TAF1/DYT3).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP735454.RAd62_jeyWn1GIbMHAtuExk2-ZO_gMcvMQMEnsWi9Xmm0130_provenance.
• assertion description "[The disease gene has been identified in 10 primary dystonias, seven autosomal dominant (TOR1A/DYT1, GCH1/DYT5a, THAP1/DYT6, PNKD1/MR-1/DYT8, SGCE/DYT11, ATP1A3/DYT12 and SLC2A1/DYT18), two autosomal recessive (TH/DYT5b and PRKRA/DYT16) and one X-chromosomal recessive (TAF1/DYT3).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[The disease gene has been identified in 10 primary dystonias, seven autosomal dominant (TOR1A/DYT1, GCH1/DYT5a, THAP1/DYT6, PNKD1/MR-1/DYT8, SGCE/DYT11, ATP1A3/DYT12 and SLC2A1/DYT18), two autosomal recessive (TH/DYT5b and PRKRA/DYT16) and one X-chromosomal recessive (TAF1/DYT3).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[The disease gene has been identified in 10 primary dystonias, seven autosomal dominant (TOR1A/DYT1, GCH1/DYT5a, THAP1/DYT6, PNKD1/MR-1/DYT8, SGCE/DYT11, ATP1A3/DYT12 and SLC2A1/DYT18), two autosomal recessive (TH/DYT5b and PRKRA/DYT16) and one X-chromosomal recessive (TAF1/DYT3).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[The disease gene has been identified in 10 primary dystonias, seven autosomal dominant (TOR1A/DYT1, GCH1/DYT5a, THAP1/DYT6, PNKD1/MR-1/DYT8, SGCE/DYT11, ATP1A3/DYT12 and SLC2A1/DYT18), two autosomal recessive (TH/DYT5b and PRKRA/DYT16) and one X-chromosomal recessive (TAF1/DYT3).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP749275.RAbyxOjht7wZASAJFQUys7EXIagKjEMx7a3Pvv2h-Cn4s130_assertion description "[The disease gene has been identified in 10 primary dystonias, seven autosomal dominant (TOR1A/DYT1, GCH1/DYT5a, THAP1/DYT6, PNKD1/MR-1/DYT8, SGCE/DYT11, ATP1A3/DYT12 and SLC2A1/DYT18), two autosomal recessive (TH/DYT5b and PRKRA/DYT16) and one X-chromosomal recessive (TAF1/DYT3).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP749275.RAbyxOjht7wZASAJFQUys7EXIagKjEMx7a3Pvv2h-Cn4s130_provenance.
• NP256184.RAC7DPpwzHxrTKfEuoxSXN7B6WnV1zrg6KXpFyOBZsNKs130_assertion description "[The disease gene has been identified in 10 primary dystonias, seven autosomal dominant (TOR1A/DYT1, GCH1/DYT5a, THAP1/DYT6, PNKD1/MR-1/DYT8, SGCE/DYT11, ATP1A3/DYT12 and SLC2A1/DYT18), two autosomal recessive (TH/DYT5b and PRKRA/DYT16) and one X-chromosomal recessive (TAF1/DYT3).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP256184.RAC7DPpwzHxrTKfEuoxSXN7B6WnV1zrg6KXpFyOBZsNKs130_provenance.
• NP722181.RABtOvUdWocvwBQM1N-gO7hMFrCvH1ADrqBAcQsEenc40130_assertion description "[The disease gene has been identified in 10 primary dystonias, seven autosomal dominant (TOR1A/DYT1, GCH1/DYT5a, THAP1/DYT6, PNKD1/MR-1/DYT8, SGCE/DYT11, ATP1A3/DYT12 and SLC2A1/DYT18), two autosomal recessive (TH/DYT5b and PRKRA/DYT16) and one X-chromosomal recessive (TAF1/DYT3).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP722181.RABtOvUdWocvwBQM1N-gO7hMFrCvH1ADrqBAcQsEenc40130_provenance.
• NP695980.RA7Vwirf6vt32gn8Yl8ivhJk0_CC_UWk1f2iSHMYJygYs130_assertion description "[The disease gene has been identified in 10 primary dystonias, seven autosomal dominant (TOR1A/DYT1, GCH1/DYT5a, THAP1/DYT6, PNKD1/MR-1/DYT8, SGCE/DYT11, ATP1A3/DYT12 and SLC2A1/DYT18), two autosomal recessive (TH/DYT5b and PRKRA/DYT16) and one X-chromosomal recessive (TAF1/DYT3).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP695980.RA7Vwirf6vt32gn8Yl8ivhJk0_CC_UWk1f2iSHMYJygYs130_provenance.
• NP749268.RAKbL0STNv930ArC5DyGIb_leBv_-OKtbdzR_M5Io8NS0130_assertion description "[The disease gene has been identified in 10 primary dystonias, seven autosomal dominant (TOR1A/DYT1, GCH1/DYT5a, THAP1/DYT6, PNKD1/MR-1/DYT8, SGCE/DYT11, ATP1A3/DYT12 and SLC2A1/DYT18), two autosomal recessive (TH/DYT5b and PRKRA/DYT16) and one X-chromosomal recessive (TAF1/DYT3).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP749268.RAKbL0STNv930ArC5DyGIb_leBv_-OKtbdzR_M5Io8NS0130_provenance.
• NP749269.RAHva7SmEPxqvhDuXsekQHxaJKTk_CbZQwAN--K1eNIoc130_assertion description "[The disease gene has been identified in 10 primary dystonias, seven autosomal dominant (TOR1A/DYT1, GCH1/DYT5a, THAP1/DYT6, PNKD1/MR-1/DYT8, SGCE/DYT11, ATP1A3/DYT12 and SLC2A1/DYT18), two autosomal recessive (TH/DYT5b and PRKRA/DYT16) and one X-chromosomal recessive (TAF1/DYT3).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP749269.RAHva7SmEPxqvhDuXsekQHxaJKTk_CbZQwAN--K1eNIoc130_provenance.
• NP749273.RAJePbhUvOaobJkFH16xOrfWNTIbSKuGK-2htB-QltJHc130_assertion description "[The disease gene has been identified in 10 primary dystonias, seven autosomal dominant (TOR1A/DYT1, GCH1/DYT5a, THAP1/DYT6, PNKD1/MR-1/DYT8, SGCE/DYT11, ATP1A3/DYT12 and SLC2A1/DYT18), two autosomal recessive (TH/DYT5b and PRKRA/DYT16) and one X-chromosomal recessive (TAF1/DYT3).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP749273.RAJePbhUvOaobJkFH16xOrfWNTIbSKuGK-2htB-QltJHc130_provenance.
• NP798791.RA_dJ4MYH0GroS4iFZ6VH4DUBchE02znj7oyBVQsouqAE130_assertion description "[The disease gene has been identified in 10 primary dystonias, seven autosomal dominant (TOR1A/DYT1, GCH1/DYT5a, THAP1/DYT6, PNKD1/MR-1/DYT8, SGCE/DYT11, ATP1A3/DYT12 and SLC2A1/DYT18), two autosomal recessive (TH/DYT5b and PRKRA/DYT16) and one X-chromosomal recessive (TAF1/DYT3).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP798791.RA_dJ4MYH0GroS4iFZ6VH4DUBchE02znj7oyBVQsouqAE130_provenance.
• NP749274.RA069qvhkG8Pkid9ztxgHfINmqhW1-s-gv44otW8HY-kc130_assertion description "[The disease gene has been identified in 10 primary dystonias, seven autosomal dominant (TOR1A/DYT1, GCH1/DYT5a, THAP1/DYT6, PNKD1/MR-1/DYT8, SGCE/DYT11, ATP1A3/DYT12 and SLC2A1/DYT18), two autosomal recessive (TH/DYT5b and PRKRA/DYT16) and one X-chromosomal recessive (TAF1/DYT3).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP749274.RA069qvhkG8Pkid9ztxgHfINmqhW1-s-gv44otW8HY-kc130_provenance.