Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP890774.RA2aW83GofmXWvqWtxoz2Y6Bb2-4tNSQvyN_SlDUPLI7s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP890774.RA2aW83GofmXWvqWtxoz2Y6Bb2-4tNSQvyN_SlDUPLI7s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP890774.RA2aW83GofmXWvqWtxoz2Y6Bb2-4tNSQvyN_SlDUPLI7s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP890774.RA2aW83GofmXWvqWtxoz2Y6Bb2-4tNSQvyN_SlDUPLI7s130_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.
- 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.
- befree-20140225 importedOn "2014-02-25" NP890774.RA2aW83GofmXWvqWtxoz2Y6Bb2-4tNSQvyN_SlDUPLI7s130_provenance.