Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[Therefore, such MPZ gene mutations should be searched for in cases of demyelinating neuropathy with acute nerve compression as well as in cases of the HNPP phenotype associated with normal the PMP22 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP298490.RAUTXOWF4RzavnIiHVSY-DJymCjZ-WXT_FNMP4dNEmpTI130_assertion description "[Therefore, such MPZ gene mutations should be searched for in cases of demyelinating neuropathy with acute nerve compression as well as in cases of the HNPP phenotype associated with normal the PMP22 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP298490.RAUTXOWF4RzavnIiHVSY-DJymCjZ-WXT_FNMP4dNEmpTI130_provenance.
• NP469876.RA0Co32g3st7vLmeltT-EhR0zNGddoARPxnyczSrNisOE130_assertion description "[Therefore, such MPZ gene mutations should be searched for in cases of demyelinating neuropathy with acute nerve compression as well as in cases of the HNPP phenotype associated with normal the PMP22 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP469876.RA0Co32g3st7vLmeltT-EhR0zNGddoARPxnyczSrNisOE130_provenance.
• NP312563.RA-XYxcOHPMgraFECGR94Fh0VcaJ2xkXMZsTrJfJjJOAc130_assertion description "[Therefore, such MPZ gene mutations should be searched for in cases of demyelinating neuropathy with acute nerve compression as well as in cases of the HNPP phenotype associated with normal the PMP22 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP312563.RA-XYxcOHPMgraFECGR94Fh0VcaJ2xkXMZsTrJfJjJOAc130_provenance.
• NP430088.RALr62dEz_xu1PZmUW9Sn6FM1KETP-482eQQXsQUSDdl8130_assertion description "[Therefore, such MPZ gene mutations should be searched for in cases of demyelinating neuropathy with acute nerve compression as well as in cases of the HNPP phenotype associated with normal the PMP22 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP430088.RALr62dEz_xu1PZmUW9Sn6FM1KETP-482eQQXsQUSDdl8130_provenance.
• NP555807.RAFl4dDiweL3mQg9GjKP_dnZgoQ0KS_K7ofT_mIRCRKPQ130_assertion description "[Therefore, such MPZ gene mutations should be searched for in cases of demyelinating neuropathy with acute nerve compression as well as in cases of the HNPP phenotype associated with normal the PMP22 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP555807.RAFl4dDiweL3mQg9GjKP_dnZgoQ0KS_K7ofT_mIRCRKPQ130_provenance.
• assertion description "[Therefore, such MPZ gene mutations should be searched for in cases of demyelinating neuropathy with acute nerve compression as well as in cases of the HNPP phenotype associated with normal the PMP22 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Therefore, such MPZ gene mutations should be searched for in cases of demyelinating neuropathy with acute nerve compression as well as in cases of the HNPP phenotype associated with normal the PMP22 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Therefore, such MPZ gene mutations should be searched for in cases of demyelinating neuropathy with acute nerve compression as well as in cases of the HNPP phenotype associated with normal the PMP22 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Therefore, such MPZ gene mutations should be searched for in cases of demyelinating neuropathy with acute nerve compression as well as in cases of the HNPP phenotype associated with normal the PMP22 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP568302.RAjNxQXc3hBXo_PsGAqQDkcej5EhiLxOspmYycuunnSds130_assertion description "[Therefore, such MPZ gene mutations should be searched for in cases of demyelinating neuropathy with acute nerve compression as well as in cases of the HNPP phenotype associated with normal the PMP22 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP568302.RAjNxQXc3hBXo_PsGAqQDkcej5EhiLxOspmYycuunnSds130_provenance.
• NP684834.RAcRevZfd_l9c57wpw_zoHYBW0NPpUjnWUPV5hf3FkTmI130_assertion description "[Therefore, such MPZ gene mutations should be searched for in cases of demyelinating neuropathy with acute nerve compression as well as in cases of the HNPP phenotype associated with normal the PMP22 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP684834.RAcRevZfd_l9c57wpw_zoHYBW0NPpUjnWUPV5hf3FkTmI130_provenance.
• NP568273.RAA9pI1DZcV_1bbH02aCHp45pf7aiUnYq94S3qGCO0EkY130_assertion description "[Therefore, such MPZ gene mutations should be searched for in cases of demyelinating neuropathy with acute nerve compression as well as in cases of the HNPP phenotype associated with normal the PMP22 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP568273.RAA9pI1DZcV_1bbH02aCHp45pf7aiUnYq94S3qGCO0EkY130_provenance.
• NP632468.RAgMPdN8t_m1tvy5ueIwEG8k6SDYWYiwDL14EdIvmmbaM130_assertion description "[Therefore, such MPZ gene mutations should be searched for in cases of demyelinating neuropathy with acute nerve compression as well as in cases of the HNPP phenotype associated with normal the PMP22 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP632468.RAgMPdN8t_m1tvy5ueIwEG8k6SDYWYiwDL14EdIvmmbaM130_provenance.
• NP662245.RAk1beJ-rjw3hDcQdl_254G8g3uWswUi-c4oOwxQPuX60130_assertion description "[Therefore, such MPZ gene mutations should be searched for in cases of demyelinating neuropathy with acute nerve compression as well as in cases of the HNPP phenotype associated with normal the PMP22 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP662245.RAk1beJ-rjw3hDcQdl_254G8g3uWswUi-c4oOwxQPuX60130_provenance.
• NP684837.RAtABTDGGIFpmkGRxzB3TsyV7MNW-r545zO91ymQUJRlI130_assertion description "[Therefore, such MPZ gene mutations should be searched for in cases of demyelinating neuropathy with acute nerve compression as well as in cases of the HNPP phenotype associated with normal the PMP22 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP684837.RAtABTDGGIFpmkGRxzB3TsyV7MNW-r545zO91ymQUJRlI130_provenance.
• NP684838.RAJo_J73IF7tc9m2trnarn4ijVVQj2hLtjxEnXlXUjrGk130_assertion description "[Therefore, such MPZ gene mutations should be searched for in cases of demyelinating neuropathy with acute nerve compression as well as in cases of the HNPP phenotype associated with normal the PMP22 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP684838.RAJo_J73IF7tc9m2trnarn4ijVVQj2hLtjxEnXlXUjrGk130_provenance.
• NP684836.RAzn_OUa2wrRlaB5NBZAjuebjslpfj5K46DAToWoGbBk0130_assertion description "[Therefore, such MPZ gene mutations should be searched for in cases of demyelinating neuropathy with acute nerve compression as well as in cases of the HNPP phenotype associated with normal the PMP22 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP684836.RAzn_OUa2wrRlaB5NBZAjuebjslpfj5K46DAToWoGbBk0130_provenance.
• NP684839.RA4Qc25EH4crlXWor2cEp5bwddsvdSBLHRSnt4FJKZ_Wo130_assertion description "[Therefore, such MPZ gene mutations should be searched for in cases of demyelinating neuropathy with acute nerve compression as well as in cases of the HNPP phenotype associated with normal the PMP22 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP684839.RA4Qc25EH4crlXWor2cEp5bwddsvdSBLHRSnt4FJKZ_Wo130_provenance.
• NP684840.RA4i5tjAF3zc6gPf01s3MwHZiRQr1BQtpUBMZDbCYwEAs130_assertion description "[Therefore, such MPZ gene mutations should be searched for in cases of demyelinating neuropathy with acute nerve compression as well as in cases of the HNPP phenotype associated with normal the PMP22 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP684840.RA4i5tjAF3zc6gPf01s3MwHZiRQr1BQtpUBMZDbCYwEAs130_provenance.