Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP435333.RAC_goblKyaDfe7DpJqCfnu4iQvLZZcaR9jrHlhcjt10o130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP435333.RAC_goblKyaDfe7DpJqCfnu4iQvLZZcaR9jrHlhcjt10o130_assertion type Assertion NP435333.RAC_goblKyaDfe7DpJqCfnu4iQvLZZcaR9jrHlhcjt10o130_head.
- NP435333.RAC_goblKyaDfe7DpJqCfnu4iQvLZZcaR9jrHlhcjt10o130_assertion wasGeneratedBy ECO_0000203 NP435333.RAC_goblKyaDfe7DpJqCfnu4iQvLZZcaR9jrHlhcjt10o130_provenance.
- NP435333.RAC_goblKyaDfe7DpJqCfnu4iQvLZZcaR9jrHlhcjt10o130_assertion wasDerivedFrom befree-20140225 NP435333.RAC_goblKyaDfe7DpJqCfnu4iQvLZZcaR9jrHlhcjt10o130_provenance.
- NP435333.RAC_goblKyaDfe7DpJqCfnu4iQvLZZcaR9jrHlhcjt10o130_assertion SIO_000772 14506070 NP435333.RAC_goblKyaDfe7DpJqCfnu4iQvLZZcaR9jrHlhcjt10o130_provenance.
- NP435333.RAC_goblKyaDfe7DpJqCfnu4iQvLZZcaR9jrHlhcjt10o130_assertion evidence source_evidence_literature NP435333.RAC_goblKyaDfe7DpJqCfnu4iQvLZZcaR9jrHlhcjt10o130_provenance.
- NP435333.RAC_goblKyaDfe7DpJqCfnu4iQvLZZcaR9jrHlhcjt10o130_assertion description "[Ataxia with ocular motor apraxia type 1 (AOA1) is an autosomal recessive cerebellar ataxia (ARCA) associated with oculomotor apraxia, hypoalbuminaemia and hypercholesterolaemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP435333.RAC_goblKyaDfe7DpJqCfnu4iQvLZZcaR9jrHlhcjt10o130_provenance.