Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[So far, disease-associated mutations have been identified in seven genes: two genes for autosomal dominant (SPTLC1 and RAB7) and five genes for autosomal recessive forms of HSAN (WNK1/HSN2, NTRK1, NGFB, CCT5 and IKBKAP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP70392.RAfoo9rHJShw9g4O-_tIWCzpf9Xjia94Of8pLsU-qp3uI130_assertion description "[So far, disease-associated mutations have been identified in seven genes: two genes for autosomal dominant (SPTLC1 and RAB7) and five genes for autosomal recessive forms of HSAN (WNK1/HSN2, NTRK1, NGFB, CCT5 and IKBKAP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP70392.RAfoo9rHJShw9g4O-_tIWCzpf9Xjia94Of8pLsU-qp3uI130_provenance.
• NP70705.RA4-_9k2pUkdyklU1JmT2q1Z7FvxFyLSaxckd_f9rNlaM130_assertion description "[So far, disease-associated mutations have been identified in seven genes: two genes for autosomal dominant (SPTLC1 and RAB7) and five genes for autosomal recessive forms of HSAN (WNK1/HSN2, NTRK1, NGFB, CCT5 and IKBKAP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP70705.RA4-_9k2pUkdyklU1JmT2q1Z7FvxFyLSaxckd_f9rNlaM130_provenance.
• NP212144.RAZveq7FC2xI3I84UFGWusYa7xC_tJS3BRq14poo3T3so130_assertion description "[So far, disease-associated mutations have been identified in seven genes: two genes for autosomal dominant (SPTLC1 and RAB7) and five genes for autosomal recessive forms of HSAN (WNK1/HSN2, NTRK1, NGFB, CCT5 and IKBKAP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP212144.RAZveq7FC2xI3I84UFGWusYa7xC_tJS3BRq14poo3T3so130_provenance.
• NP78848.RA8lfb7-rVP4M7kSGUMHXbSHRKRdxo3d345U8fl4p1cMY130_assertion description "[So far, disease-associated mutations have been identified in seven genes: two genes for autosomal dominant (SPTLC1 and RAB7) and five genes for autosomal recessive forms of HSAN (WNK1/HSN2, NTRK1, NGFB, CCT5 and IKBKAP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP78848.RA8lfb7-rVP4M7kSGUMHXbSHRKRdxo3d345U8fl4p1cMY130_provenance.
• NP72756.RAhMPLjTNPlv-0iD5lz-DzNtGkET00kpF8bpyTjf44JkE130_assertion description "[So far, disease-associated mutations have been identified in seven genes: two genes for autosomal dominant (SPTLC1 and RAB7) and five genes for autosomal recessive forms of HSAN (WNK1/HSN2, NTRK1, NGFB, CCT5 and IKBKAP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP72756.RAhMPLjTNPlv-0iD5lz-DzNtGkET00kpF8bpyTjf44JkE130_provenance.
• NP298248.RAs4f-t7hfWzDUL4bDDd0HO-xeu14IpZL8r4PpZ3zJF8E130_assertion description "[So far, disease-associated mutations have been identified in seven genes: two genes for autosomal dominant (SPTLC1 and RAB7) and five genes for autosomal recessive forms of HSAN (WNK1/HSN2, NTRK1, NGFB, CCT5 and IKBKAP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP298248.RAs4f-t7hfWzDUL4bDDd0HO-xeu14IpZL8r4PpZ3zJF8E130_provenance.
• NP68730.RAE7EW6ibaZo69Y5yQdIxx9XeyEST9QjPwGftzwK2q69A130_assertion description "[So far, disease-associated mutations have been identified in seven genes: two genes for autosomal dominant (SPTLC1 and RAB7) and five genes for autosomal recessive forms of HSAN (WNK1/HSN2, NTRK1, NGFB, CCT5 and IKBKAP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP68730.RAE7EW6ibaZo69Y5yQdIxx9XeyEST9QjPwGftzwK2q69A130_provenance.
• NP70979.RAs7FzdivjX874NdCPzc9GoznAvguI_DjPHwTL8Xa_ZwA130_assertion description "[So far, disease-associated mutations have been identified in seven genes: two genes for autosomal dominant (SPTLC1 and RAB7) and five genes for autosomal recessive forms of HSAN (WNK1/HSN2, NTRK1, NGFB, CCT5 and IKBKAP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP70979.RAs7FzdivjX874NdCPzc9GoznAvguI_DjPHwTL8Xa_ZwA130_provenance.
• NP466599.RAWS4zV3x6zceUYvqWRGsS8h_-S-sMpQ6bm3Kz9kTAtvs130_assertion description "[So far, disease-associated mutations have been identified in seven genes: two genes for autosomal dominant (SPTLC1 and RAB7) and five genes for autosomal recessive forms of HSAN (WNK1/HSN2, NTRK1, NGFB, CCT5 and IKBKAP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP466599.RAWS4zV3x6zceUYvqWRGsS8h_-S-sMpQ6bm3Kz9kTAtvs130_provenance.
• NP95116.RAe9lJK2nr-RKeoWaO7X8XDOTlssXstiLxyn_rE4VrYtI130_assertion description "[So far, disease-associated mutations have been identified in seven genes: two genes for autosomal dominant (SPTLC1 and RAB7) and five genes for autosomal recessive forms of HSAN (WNK1/HSN2, NTRK1, NGFB, CCT5 and IKBKAP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP95116.RAe9lJK2nr-RKeoWaO7X8XDOTlssXstiLxyn_rE4VrYtI130_provenance.
• NP101431.RAZCGpUhXIsqUIVGcgtNjQqN591IsnTXkFhzINj7QDgQ8130_assertion description "[So far, disease-associated mutations have been identified in seven genes: two genes for autosomal dominant (SPTLC1 and RAB7) and five genes for autosomal recessive forms of HSAN (WNK1/HSN2, NTRK1, NGFB, CCT5 and IKBKAP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP101431.RAZCGpUhXIsqUIVGcgtNjQqN591IsnTXkFhzINj7QDgQ8130_provenance.
• NP742988.RA9mqeWn0NXH1DASeEQrB0m-0XvjshAYghwZzf8kctDNo130_assertion description "[So far, disease-associated mutations have been identified in seven genes: two genes for autosomal dominant (SPTLC1 and RAB7) and five genes for autosomal recessive forms of HSAN (WNK1/HSN2, NTRK1, NGFB, CCT5 and IKBKAP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP742988.RA9mqeWn0NXH1DASeEQrB0m-0XvjshAYghwZzf8kctDNo130_provenance.
• assertion description "[So far, disease-associated mutations have been identified in seven genes: two genes for autosomal dominant (SPTLC1 and RAB7) and five genes for autosomal recessive forms of HSAN (WNK1/HSN2, NTRK1, NGFB, CCT5 and IKBKAP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP985191.RAbFdRQIraSFc3Gkm0t60bhxKeycIb6mrq_U03x03nN3U130_assertion description "[So far, disease-associated mutations have been identified in seven genes: two genes for autosomal dominant (SPTLC1 and RAB7) and five genes for autosomal recessive forms of HSAN (WNK1/HSN2, NTRK1, NGFB, CCT5 and IKBKAP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP985191.RAbFdRQIraSFc3Gkm0t60bhxKeycIb6mrq_U03x03nN3U130_provenance.
• assertion description "[So far, disease-associated mutations have been identified in seven genes: two genes for autosomal dominant (SPTLC1 and RAB7) and five genes for autosomal recessive forms of HSAN (WNK1/HSN2, NTRK1, NGFB, CCT5 and IKBKAP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP117321.RAl8Q5PKU69Smk__oLkWtPS31YTEAV5_ncrjHulhX7Cqw130_assertion description "[So far, disease-associated mutations have been identified in seven genes: two genes for autosomal dominant (SPTLC1 and RAB7) and five genes for autosomal recessive forms of HSAN (WNK1/HSN2, NTRK1, NGFB, CCT5 and IKBKAP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP117321.RAl8Q5PKU69Smk__oLkWtPS31YTEAV5_ncrjHulhX7Cqw130_provenance.
• assertion description "[So far, disease-associated mutations have been identified in seven genes: two genes for autosomal dominant (SPTLC1 and RAB7) and five genes for autosomal recessive forms of HSAN (WNK1/HSN2, NTRK1, NGFB, CCT5 and IKBKAP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP153874.RAYl3Dg3hOEWwgcfiMX86-cfCcFE3MtdxghwXuDv-GljY130_assertion description "[So far, disease-associated mutations have been identified in seven genes: two genes for autosomal dominant (SPTLC1 and RAB7) and five genes for autosomal recessive forms of HSAN (WNK1/HSN2, NTRK1, NGFB, CCT5 and IKBKAP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP153874.RAYl3Dg3hOEWwgcfiMX86-cfCcFE3MtdxghwXuDv-GljY130_provenance.
• NP89718.RAloCELpNScN4Wj_6VWU0IkMxVFJasQHZqHvBGk58XdcY130_assertion description "[So far, disease-associated mutations have been identified in seven genes: two genes for autosomal dominant (SPTLC1 and RAB7) and five genes for autosomal recessive forms of HSAN (WNK1/HSN2, NTRK1, NGFB, CCT5 and IKBKAP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89718.RAloCELpNScN4Wj_6VWU0IkMxVFJasQHZqHvBGk58XdcY130_provenance.
• assertion description "[So far, disease-associated mutations have been identified in seven genes: two genes for autosomal dominant (SPTLC1 and RAB7) and five genes for autosomal recessive forms of HSAN (WNK1/HSN2, NTRK1, NGFB, CCT5 and IKBKAP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[So far, disease-associated mutations have been identified in seven genes: two genes for autosomal dominant (SPTLC1 and RAB7) and five genes for autosomal recessive forms of HSAN (WNK1/HSN2, NTRK1, NGFB, CCT5 and IKBKAP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[So far, disease-associated mutations have been identified in seven genes: two genes for autosomal dominant (SPTLC1 and RAB7) and five genes for autosomal recessive forms of HSAN (WNK1/HSN2, NTRK1, NGFB, CCT5 and IKBKAP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[So far, disease-associated mutations have been identified in seven genes: two genes for autosomal dominant (SPTLC1 and RAB7) and five genes for autosomal recessive forms of HSAN (WNK1/HSN2, NTRK1, NGFB, CCT5 and IKBKAP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP722922.RAOM0bLwfluluq8qBPpPBMwR0DUFibVerVn_azyIdvoJ4130_assertion description "[So far, disease-associated mutations have been identified in seven genes: two genes for autosomal dominant (SPTLC1 and RAB7) and five genes for autosomal recessive forms of HSAN (WNK1/HSN2, NTRK1, NGFB, CCT5 and IKBKAP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP722922.RAOM0bLwfluluq8qBPpPBMwR0DUFibVerVn_azyIdvoJ4130_provenance.
• assertion description "[So far, disease-associated mutations have been identified in seven genes: two genes for autosomal dominant (SPTLC1 and RAB7) and five genes for autosomal recessive forms of HSAN (WNK1/HSN2, NTRK1, NGFB, CCT5 and IKBKAP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP755125.RAA-Zmg8zwKKmshtQUYumyQjDIFa2cPtwuDACERED6bmE130_assertion description "[So far, disease-associated mutations have been identified in seven genes: two genes for autosomal dominant (SPTLC1 and RAB7) and five genes for autosomal recessive forms of HSAN (WNK1/HSN2, NTRK1, NGFB, CCT5 and IKBKAP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP755125.RAA-Zmg8zwKKmshtQUYumyQjDIFa2cPtwuDACERED6bmE130_provenance.
• NP755131.RAU03kG1c8Tkpw4zA1siOSQr-UgBNUuW_3xh_BRADysP4130_assertion description "[So far, disease-associated mutations have been identified in seven genes: two genes for autosomal dominant (SPTLC1 and RAB7) and five genes for autosomal recessive forms of HSAN (WNK1/HSN2, NTRK1, NGFB, CCT5 and IKBKAP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP755131.RAU03kG1c8Tkpw4zA1siOSQr-UgBNUuW_3xh_BRADysP4130_provenance.
• assertion description "[So far, disease-associated mutations have been identified in seven genes: two genes for autosomal dominant (SPTLC1 and RAB7) and five genes for autosomal recessive forms of HSAN (WNK1/HSN2, NTRK1, NGFB, CCT5 and IKBKAP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[So far, disease-associated mutations have been identified in seven genes: two genes for autosomal dominant (SPTLC1 and RAB7) and five genes for autosomal recessive forms of HSAN (WNK1/HSN2, NTRK1, NGFB, CCT5 and IKBKAP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP941263.RAAqnw1WyAYYtvDWqoISIG6uuKYFcDmV0F7Y1JTnQFexs130_assertion description "[So far, disease-associated mutations have been identified in seven genes: two genes for autosomal dominant (SPTLC1 and RAB7) and five genes for autosomal recessive forms of HSAN (WNK1/HSN2, NTRK1, NGFB, CCT5 and IKBKAP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP941263.RAAqnw1WyAYYtvDWqoISIG6uuKYFcDmV0F7Y1JTnQFexs130_provenance.
• NP785687.RAswkWDoFdxrLEBe4fSGAcVJj-T9YRVFnz3Yr2qr5FVGg130_assertion description "[So far, disease-associated mutations have been identified in seven genes: two genes for autosomal dominant (SPTLC1 and RAB7) and five genes for autosomal recessive forms of HSAN (WNK1/HSN2, NTRK1, NGFB, CCT5 and IKBKAP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP785687.RAswkWDoFdxrLEBe4fSGAcVJj-T9YRVFnz3Yr2qr5FVGg130_provenance.
• NP814672.RAKXcq56g2hsElsNgmSCZTweFOdF-dwOyZ8Msv7bOzbm0130_assertion description "[So far, disease-associated mutations have been identified in seven genes: two genes for autosomal dominant (SPTLC1 and RAB7) and five genes for autosomal recessive forms of HSAN (WNK1/HSN2, NTRK1, NGFB, CCT5 and IKBKAP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP814672.RAKXcq56g2hsElsNgmSCZTweFOdF-dwOyZ8Msv7bOzbm0130_provenance.
• NP95867.RAOz5aNc8_Y_PDA4b89x-5g92iBK_PS4vnHkJxeGGi8E8130_assertion description "[So far, disease-associated mutations have been identified in seven genes: two genes for autosomal dominant (SPTLC1 and RAB7) and five genes for autosomal recessive forms of HSAN (WNK1/HSN2, NTRK1, NGFB, CCT5 and IKBKAP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP95867.RAOz5aNc8_Y_PDA4b89x-5g92iBK_PS4vnHkJxeGGi8E8130_provenance.
• NP153871.RAjCzqD3Hd_saJeV57si-gqOpWI2Z42Fkxh2Lemmnn8Ls130_assertion description "[So far, disease-associated mutations have been identified in seven genes: two genes for autosomal dominant (SPTLC1 and RAB7) and five genes for autosomal recessive forms of HSAN (WNK1/HSN2, NTRK1, NGFB, CCT5 and IKBKAP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP153871.RAjCzqD3Hd_saJeV57si-gqOpWI2Z42Fkxh2Lemmnn8Ls130_provenance.
• NP153872.RAuwrEN5LNL4KoLmv3uaVOwu8UbojCl2iQv1zNShSAOYE130_assertion description "[So far, disease-associated mutations have been identified in seven genes: two genes for autosomal dominant (SPTLC1 and RAB7) and five genes for autosomal recessive forms of HSAN (WNK1/HSN2, NTRK1, NGFB, CCT5 and IKBKAP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP153872.RAuwrEN5LNL4KoLmv3uaVOwu8UbojCl2iQv1zNShSAOYE130_provenance.
• NP94465.RA6IIV8GpXP5pZQYoFRZ0FBGXqVTF3iyaL-cMIq7Cz2CI130_assertion description "[So far, disease-associated mutations have been identified in seven genes: two genes for autosomal dominant (SPTLC1 and RAB7) and five genes for autosomal recessive forms of HSAN (WNK1/HSN2, NTRK1, NGFB, CCT5 and IKBKAP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP94465.RA6IIV8GpXP5pZQYoFRZ0FBGXqVTF3iyaL-cMIq7Cz2CI130_provenance.
• NP755134.RAsixUhsWAyDDE2RG91fxF1pgbyc7lLRVseadOWtWKCJ8130_assertion description "[So far, disease-associated mutations have been identified in seven genes: two genes for autosomal dominant (SPTLC1 and RAB7) and five genes for autosomal recessive forms of HSAN (WNK1/HSN2, NTRK1, NGFB, CCT5 and IKBKAP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP755134.RAsixUhsWAyDDE2RG91fxF1pgbyc7lLRVseadOWtWKCJ8130_provenance.
• NP797522.RA6Z21LItJBvZTfwi7-IgPDvwqC2taNw0rWNhkbRMXVw8130_assertion description "[So far, disease-associated mutations have been identified in seven genes: two genes for autosomal dominant (SPTLC1 and RAB7) and five genes for autosomal recessive forms of HSAN (WNK1/HSN2, NTRK1, NGFB, CCT5 and IKBKAP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP797522.RA6Z21LItJBvZTfwi7-IgPDvwqC2taNw0rWNhkbRMXVw8130_provenance.
• NP153868.RA0LgaKe3rnL72CK9U0uBi-SNvf2LGj4zivf-TKh0afZM130_assertion description "[So far, disease-associated mutations have been identified in seven genes: two genes for autosomal dominant (SPTLC1 and RAB7) and five genes for autosomal recessive forms of HSAN (WNK1/HSN2, NTRK1, NGFB, CCT5 and IKBKAP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP153868.RA0LgaKe3rnL72CK9U0uBi-SNvf2LGj4zivf-TKh0afZM130_provenance.
• NP153869.RA16kf77jhbbt1VPKp8nMkMjuTr1NM6MNlsjO5KG69n4c130_assertion description "[So far, disease-associated mutations have been identified in seven genes: two genes for autosomal dominant (SPTLC1 and RAB7) and five genes for autosomal recessive forms of HSAN (WNK1/HSN2, NTRK1, NGFB, CCT5 and IKBKAP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP153869.RA16kf77jhbbt1VPKp8nMkMjuTr1NM6MNlsjO5KG69n4c130_provenance.
• NP153870.RA6PGhyHU1GsXleIDUDDFzPoPO04YC4_BSkaqtqgUs_-I130_assertion description "[So far, disease-associated mutations have been identified in seven genes: two genes for autosomal dominant (SPTLC1 and RAB7) and five genes for autosomal recessive forms of HSAN (WNK1/HSN2, NTRK1, NGFB, CCT5 and IKBKAP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP153870.RA6PGhyHU1GsXleIDUDDFzPoPO04YC4_BSkaqtqgUs_-I130_provenance.
• NP755128.RA7CoTsyWEf_WZ2iVCVLRIyvpB1NjzwM1Hf3-KfByJhD0130_assertion description "[So far, disease-associated mutations have been identified in seven genes: two genes for autosomal dominant (SPTLC1 and RAB7) and five genes for autosomal recessive forms of HSAN (WNK1/HSN2, NTRK1, NGFB, CCT5 and IKBKAP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP755128.RA7CoTsyWEf_WZ2iVCVLRIyvpB1NjzwM1Hf3-KfByJhD0130_provenance.