Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP6579.RAei7Tq2lsYCgIFWAvF7WcaLn5NpVvw2G8snVsOAdAajs130_assertion> ?p ?o ?g. }
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- NP6579.RAei7Tq2lsYCgIFWAvF7WcaLn5NpVvw2G8snVsOAdAajs130_assertion type Assertion NP6579.RAei7Tq2lsYCgIFWAvF7WcaLn5NpVvw2G8snVsOAdAajs130_head.
- NP6579.RAei7Tq2lsYCgIFWAvF7WcaLn5NpVvw2G8snVsOAdAajs130_assertion description "[A common point mutation in the tyrosine hydroxylase gene in autosomal recessive L-DOPA-responsive dystonia in the Dutch population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP6579.RAei7Tq2lsYCgIFWAvF7WcaLn5NpVvw2G8snVsOAdAajs130_provenance.
- NP6579.RAei7Tq2lsYCgIFWAvF7WcaLn5NpVvw2G8snVsOAdAajs130_assertion evidence source_evidence_curated NP6579.RAei7Tq2lsYCgIFWAvF7WcaLn5NpVvw2G8snVsOAdAajs130_provenance.
- NP6579.RAei7Tq2lsYCgIFWAvF7WcaLn5NpVvw2G8snVsOAdAajs130_assertion SIO_000772 9703425 NP6579.RAei7Tq2lsYCgIFWAvF7WcaLn5NpVvw2G8snVsOAdAajs130_provenance.
- NP6579.RAei7Tq2lsYCgIFWAvF7WcaLn5NpVvw2G8snVsOAdAajs130_assertion wasDerivedFrom uniprot-20130724 NP6579.RAei7Tq2lsYCgIFWAvF7WcaLn5NpVvw2G8snVsOAdAajs130_provenance.
- NP6579.RAei7Tq2lsYCgIFWAvF7WcaLn5NpVvw2G8snVsOAdAajs130_assertion wasGeneratedBy ECO_0000218 NP6579.RAei7Tq2lsYCgIFWAvF7WcaLn5NpVvw2G8snVsOAdAajs130_provenance.