Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP428885.RAlchZrelQnzwC7rseTW8rjGPinP8R5H6BjBM2upv-dSg130_assertion> ?p ?o ?g. }
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- NP428885.RAlchZrelQnzwC7rseTW8rjGPinP8R5H6BjBM2upv-dSg130_assertion type Assertion NP428885.RAlchZrelQnzwC7rseTW8rjGPinP8R5H6BjBM2upv-dSg130_head.
- NP428885.RAlchZrelQnzwC7rseTW8rjGPinP8R5H6BjBM2upv-dSg130_assertion description "[GLRB itself does not seem to be a good candidate as it causes autosomal recessive hyperekplexia and no symptoms were found in the patient.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP428885.RAlchZrelQnzwC7rseTW8rjGPinP8R5H6BjBM2upv-dSg130_provenance.
- NP428885.RAlchZrelQnzwC7rseTW8rjGPinP8R5H6BjBM2upv-dSg130_assertion evidence source_evidence_literature NP428885.RAlchZrelQnzwC7rseTW8rjGPinP8R5H6BjBM2upv-dSg130_provenance.
- NP428885.RAlchZrelQnzwC7rseTW8rjGPinP8R5H6BjBM2upv-dSg130_assertion SIO_000772 22669415 NP428885.RAlchZrelQnzwC7rseTW8rjGPinP8R5H6BjBM2upv-dSg130_provenance.
- NP428885.RAlchZrelQnzwC7rseTW8rjGPinP8R5H6BjBM2upv-dSg130_assertion wasDerivedFrom befree-20150227 NP428885.RAlchZrelQnzwC7rseTW8rjGPinP8R5H6BjBM2upv-dSg130_provenance.
- NP428885.RAlchZrelQnzwC7rseTW8rjGPinP8R5H6BjBM2upv-dSg130_assertion wasGeneratedBy ECO_0000203 NP428885.RAlchZrelQnzwC7rseTW8rjGPinP8R5H6BjBM2upv-dSg130_provenance.