Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP890774.RA2aW83GofmXWvqWtxoz2Y6Bb2-4tNSQvyN_SlDUPLI7s130_assertion> ?p ?o ?g. }
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- NP890774.RA2aW83GofmXWvqWtxoz2Y6Bb2-4tNSQvyN_SlDUPLI7s130_assertion type Assertion NP890774.RA2aW83GofmXWvqWtxoz2Y6Bb2-4tNSQvyN_SlDUPLI7s130_head.
- 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.
- NP890774.RA2aW83GofmXWvqWtxoz2Y6Bb2-4tNSQvyN_SlDUPLI7s130_assertion evidence source_evidence_literature NP890774.RA2aW83GofmXWvqWtxoz2Y6Bb2-4tNSQvyN_SlDUPLI7s130_provenance.
- NP890774.RA2aW83GofmXWvqWtxoz2Y6Bb2-4tNSQvyN_SlDUPLI7s130_assertion SIO_000772 7925268 NP890774.RA2aW83GofmXWvqWtxoz2Y6Bb2-4tNSQvyN_SlDUPLI7s130_provenance.
- NP890774.RA2aW83GofmXWvqWtxoz2Y6Bb2-4tNSQvyN_SlDUPLI7s130_assertion wasDerivedFrom befree-20140225 NP890774.RA2aW83GofmXWvqWtxoz2Y6Bb2-4tNSQvyN_SlDUPLI7s130_provenance.
- NP890774.RA2aW83GofmXWvqWtxoz2Y6Bb2-4tNSQvyN_SlDUPLI7s130_assertion wasGeneratedBy ECO_0000203 NP890774.RA2aW83GofmXWvqWtxoz2Y6Bb2-4tNSQvyN_SlDUPLI7s130_provenance.