Matches in Nanopublications for { ?s ?p "[Hereditary hyperekplexia is a dominant neurological disorder associated with point mutations at the channel-forming segment M2 of the glycine receptor alpha 1 subunit.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP2810.RA_4_Ocl3i8MnjTOCHEi2_hMCFp9FQUbiGkNI0y6-Lz4o130_assertion description "[Hereditary hyperekplexia is a dominant neurological disorder associated with point mutations at the channel-forming segment M2 of the glycine receptor alpha 1 subunit.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP2810.RA_4_Ocl3i8MnjTOCHEi2_hMCFp9FQUbiGkNI0y6-Lz4o130_provenance.
- assertion description "[Hereditary hyperekplexia is a dominant neurological disorder associated with point mutations at the channel-forming segment M2 of the glycine receptor alpha 1 subunit.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Hereditary hyperekplexia is a dominant neurological disorder associated with point mutations at the channel-forming segment M2 of the glycine receptor alpha 1 subunit.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Hereditary hyperekplexia is a dominant neurological disorder associated with point mutations at the channel-forming segment M2 of the glycine receptor alpha 1 subunit.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP890774.RA2aW83GofmXWvqWtxoz2Y6Bb2-4tNSQvyN_SlDUPLI7s130_assertion description "[Hereditary hyperekplexia is a dominant neurological disorder associated with point mutations at the channel-forming segment M2 of the glycine receptor alpha 1 subunit.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP890774.RA2aW83GofmXWvqWtxoz2Y6Bb2-4tNSQvyN_SlDUPLI7s130_provenance.
- NP1327181.RAWKc0Nj-3L5n9mI-tY_L-VmWFkDggdI7srSwuZjkv8oc130_assertion description "[Hereditary hyperekplexia is a dominant neurological disorder associated with point mutations at the channel-forming segment M2 of the glycine receptor alpha 1 subunit.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1327181.RAWKc0Nj-3L5n9mI-tY_L-VmWFkDggdI7srSwuZjkv8oc130_provenance.
- NP728961.RAMO3lDvz3laOFTR78gdcKLOyBbQb5LaORZzYRrm6YZAY130_assertion description "[Hereditary hyperekplexia is a dominant neurological disorder associated with point mutations at the channel-forming segment M2 of the glycine receptor alpha 1 subunit.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP728961.RAMO3lDvz3laOFTR78gdcKLOyBbQb5LaORZzYRrm6YZAY130_provenance.
- NP428838.RAnxKxICRXcSngNkCPJzmxi4-H4eXaQigzJhPSHTN8nrE130_assertion description "[Hereditary hyperekplexia is a dominant neurological disorder associated with point mutations at the channel-forming segment M2 of the glycine receptor alpha 1 subunit.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP428838.RAnxKxICRXcSngNkCPJzmxi4-H4eXaQigzJhPSHTN8nrE130_provenance.
- NP1327180.RAwEeu5c9ezxrdxSCmTp3CpE9YS0vwWcQkpw2mw61jbho130_assertion description "[Hereditary hyperekplexia is a dominant neurological disorder associated with point mutations at the channel-forming segment M2 of the glycine receptor alpha 1 subunit.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1327180.RAwEeu5c9ezxrdxSCmTp3CpE9YS0vwWcQkpw2mw61jbho130_provenance.