Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP914753.RABq0qxs5GDjn0zBW8ga6TEAax12rruQdj-BnigiyT7qo130_assertion> ?p ?o ?g. }
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- NP914753.RABq0qxs5GDjn0zBW8ga6TEAax12rruQdj-BnigiyT7qo130_assertion type Assertion NP914753.RABq0qxs5GDjn0zBW8ga6TEAax12rruQdj-BnigiyT7qo130_head.
- NP914753.RABq0qxs5GDjn0zBW8ga6TEAax12rruQdj-BnigiyT7qo130_assertion wasGeneratedBy ECO_0000203 NP914753.RABq0qxs5GDjn0zBW8ga6TEAax12rruQdj-BnigiyT7qo130_provenance.
- NP914753.RABq0qxs5GDjn0zBW8ga6TEAax12rruQdj-BnigiyT7qo130_assertion wasDerivedFrom befree-20150227 NP914753.RABq0qxs5GDjn0zBW8ga6TEAax12rruQdj-BnigiyT7qo130_provenance.
- NP914753.RABq0qxs5GDjn0zBW8ga6TEAax12rruQdj-BnigiyT7qo130_assertion SIO_000772 14506070 NP914753.RABq0qxs5GDjn0zBW8ga6TEAax12rruQdj-BnigiyT7qo130_provenance.
- NP914753.RABq0qxs5GDjn0zBW8ga6TEAax12rruQdj-BnigiyT7qo130_assertion evidence source_evidence_literature NP914753.RABq0qxs5GDjn0zBW8ga6TEAax12rruQdj-BnigiyT7qo130_provenance.
- NP914753.RABq0qxs5GDjn0zBW8ga6TEAax12rruQdj-BnigiyT7qo130_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." NP914753.RABq0qxs5GDjn0zBW8ga6TEAax12rruQdj-BnigiyT7qo130_provenance.