Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1114912.RAcKtdLjO-P425dTTJ16n_kIqEtgR57tZtsB2JhUWs6oM130_assertion> ?p ?o ?g. }
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- NP1114912.RAcKtdLjO-P425dTTJ16n_kIqEtgR57tZtsB2JhUWs6oM130_assertion type Assertion NP1114912.RAcKtdLjO-P425dTTJ16n_kIqEtgR57tZtsB2JhUWs6oM130_head.
- NP1114912.RAcKtdLjO-P425dTTJ16n_kIqEtgR57tZtsB2JhUWs6oM130_assertion description "[Deletions in GRID2 lead to a recessive syndrome of cerebellar ataxia and tonic upgaze in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1114912.RAcKtdLjO-P425dTTJ16n_kIqEtgR57tZtsB2JhUWs6oM130_provenance.
- NP1114912.RAcKtdLjO-P425dTTJ16n_kIqEtgR57tZtsB2JhUWs6oM130_assertion evidence source_evidence_literature NP1114912.RAcKtdLjO-P425dTTJ16n_kIqEtgR57tZtsB2JhUWs6oM130_provenance.
- NP1114912.RAcKtdLjO-P425dTTJ16n_kIqEtgR57tZtsB2JhUWs6oM130_assertion SIO_000772 24078737 NP1114912.RAcKtdLjO-P425dTTJ16n_kIqEtgR57tZtsB2JhUWs6oM130_provenance.
- NP1114912.RAcKtdLjO-P425dTTJ16n_kIqEtgR57tZtsB2JhUWs6oM130_assertion wasDerivedFrom befree-2016 NP1114912.RAcKtdLjO-P425dTTJ16n_kIqEtgR57tZtsB2JhUWs6oM130_provenance.
- NP1114912.RAcKtdLjO-P425dTTJ16n_kIqEtgR57tZtsB2JhUWs6oM130_assertion wasGeneratedBy ECO_0000203 NP1114912.RAcKtdLjO-P425dTTJ16n_kIqEtgR57tZtsB2JhUWs6oM130_provenance.