Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[Disorders with a known molecular basis falling within this group include hereditary neuropathy with liability to pressure palsies (HNPP) due to the deletion of the PMP22 gene or to mutations in this same gene, and hereditary neuralgic amyotrophy (HNA) caused by mutations in the SEPT9 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• assertion description "[Disorders with a known molecular basis falling within this group include hereditary neuropathy with liability to pressure palsies (HNPP) due to the deletion of the PMP22 gene or to mutations in this same gene, and hereditary neuralgic amyotrophy (HNA) caused by mutations in the SEPT9 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Disorders with a known molecular basis falling within this group include hereditary neuropathy with liability to pressure palsies (HNPP) due to the deletion of the PMP22 gene or to mutations in this same gene, and hereditary neuralgic amyotrophy (HNA) caused by mutations in the SEPT9 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Disorders with a known molecular basis falling within this group include hereditary neuropathy with liability to pressure palsies (HNPP) due to the deletion of the PMP22 gene or to mutations in this same gene, and hereditary neuralgic amyotrophy (HNA) caused by mutations in the SEPT9 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP1186883.RAbMaLNKJ2cRcxWJYzYLGfAWNCoKF1i5GfhpE8bDLzCJE130_assertion description "[Disorders with a known molecular basis falling within this group include hereditary neuropathy with liability to pressure palsies (HNPP) due to the deletion of the PMP22 gene or to mutations in this same gene, and hereditary neuralgic amyotrophy (HNA) caused by mutations in the SEPT9 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1186883.RAbMaLNKJ2cRcxWJYzYLGfAWNCoKF1i5GfhpE8bDLzCJE130_provenance.
• NP1186888.RABCojgUe6PS2vIJd6XYB5qAWCR5zJOhp0DGOa1TEgeGY130_assertion description "[Disorders with a known molecular basis falling within this group include hereditary neuropathy with liability to pressure palsies (HNPP) due to the deletion of the PMP22 gene or to mutations in this same gene, and hereditary neuralgic amyotrophy (HNA) caused by mutations in the SEPT9 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1186888.RABCojgUe6PS2vIJd6XYB5qAWCR5zJOhp0DGOa1TEgeGY130_provenance.
• NP1186889.RACNZYQ9ULwBKN8IWQqw-iOVP9n5fcjPjgI-CJ_RQkB5s130_assertion description "[Disorders with a known molecular basis falling within this group include hereditary neuropathy with liability to pressure palsies (HNPP) due to the deletion of the PMP22 gene or to mutations in this same gene, and hereditary neuralgic amyotrophy (HNA) caused by mutations in the SEPT9 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1186889.RACNZYQ9ULwBKN8IWQqw-iOVP9n5fcjPjgI-CJ_RQkB5s130_provenance.
• NP1186886.RAIKPJdazaBdHmYpKBCH2c0bejBxul00vdiROX7xQydAE130_assertion description "[Disorders with a known molecular basis falling within this group include hereditary neuropathy with liability to pressure palsies (HNPP) due to the deletion of the PMP22 gene or to mutations in this same gene, and hereditary neuralgic amyotrophy (HNA) caused by mutations in the SEPT9 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1186886.RAIKPJdazaBdHmYpKBCH2c0bejBxul00vdiROX7xQydAE130_provenance.
• NP1186885.RA0E0WQYz4PUkIpfwqki7AlGGi59SrsRVIjBaHdVSZWMk130_assertion description "[Disorders with a known molecular basis falling within this group include hereditary neuropathy with liability to pressure palsies (HNPP) due to the deletion of the PMP22 gene or to mutations in this same gene, and hereditary neuralgic amyotrophy (HNA) caused by mutations in the SEPT9 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1186885.RA0E0WQYz4PUkIpfwqki7AlGGi59SrsRVIjBaHdVSZWMk130_provenance.
• NP1186887.RA-yg612_PCPSA131QDlYXei7uXfGicDVwVvdKL_EtB4c130_assertion description "[Disorders with a known molecular basis falling within this group include hereditary neuropathy with liability to pressure palsies (HNPP) due to the deletion of the PMP22 gene or to mutations in this same gene, and hereditary neuralgic amyotrophy (HNA) caused by mutations in the SEPT9 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1186887.RA-yg612_PCPSA131QDlYXei7uXfGicDVwVvdKL_EtB4c130_provenance.