Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1260237.RAThm_m2Y65_LELuEAux_X6y5ipRqFQBcmSgbwsYnDjWY130_assertion> ?p ?o ?g. }
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- NP1260237.RAThm_m2Y65_LELuEAux_X6y5ipRqFQBcmSgbwsYnDjWY130_assertion type Assertion NP1260237.RAThm_m2Y65_LELuEAux_X6y5ipRqFQBcmSgbwsYnDjWY130_head.
- NP1260237.RAThm_m2Y65_LELuEAux_X6y5ipRqFQBcmSgbwsYnDjWY130_assertion description "[Similarly, ATP1A3 mutations cause a wide phenotypic spectrum ranging from rapid-onset dystonia-parkinsonism to alternating hemiplegia of childhood.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1260237.RAThm_m2Y65_LELuEAux_X6y5ipRqFQBcmSgbwsYnDjWY130_provenance.
- NP1260237.RAThm_m2Y65_LELuEAux_X6y5ipRqFQBcmSgbwsYnDjWY130_assertion evidence source_evidence_literature NP1260237.RAThm_m2Y65_LELuEAux_X6y5ipRqFQBcmSgbwsYnDjWY130_provenance.
- NP1260237.RAThm_m2Y65_LELuEAux_X6y5ipRqFQBcmSgbwsYnDjWY130_assertion SIO_000772 25643588 NP1260237.RAThm_m2Y65_LELuEAux_X6y5ipRqFQBcmSgbwsYnDjWY130_provenance.
- NP1260237.RAThm_m2Y65_LELuEAux_X6y5ipRqFQBcmSgbwsYnDjWY130_assertion wasDerivedFrom befree-2016 NP1260237.RAThm_m2Y65_LELuEAux_X6y5ipRqFQBcmSgbwsYnDjWY130_provenance.
- NP1260237.RAThm_m2Y65_LELuEAux_X6y5ipRqFQBcmSgbwsYnDjWY130_assertion wasGeneratedBy ECO_0000203 NP1260237.RAThm_m2Y65_LELuEAux_X6y5ipRqFQBcmSgbwsYnDjWY130_provenance.