Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP235407.RANolmCmmhPQXmPeOSi2R-gKx0ZAZeQKUi0ew7qwIsJIk130_assertion> ?p ?o ?g. }
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- NP235407.RANolmCmmhPQXmPeOSi2R-gKx0ZAZeQKUi0ew7qwIsJIk130_assertion type Assertion NP235407.RANolmCmmhPQXmPeOSi2R-gKx0ZAZeQKUi0ew7qwIsJIk130_head.
- NP235407.RANolmCmmhPQXmPeOSi2R-gKx0ZAZeQKUi0ew7qwIsJIk130_assertion wasGeneratedBy ECO_0000203 NP235407.RANolmCmmhPQXmPeOSi2R-gKx0ZAZeQKUi0ew7qwIsJIk130_provenance.
- NP235407.RANolmCmmhPQXmPeOSi2R-gKx0ZAZeQKUi0ew7qwIsJIk130_assertion wasDerivedFrom befree-20140225 NP235407.RANolmCmmhPQXmPeOSi2R-gKx0ZAZeQKUi0ew7qwIsJIk130_provenance.
- NP235407.RANolmCmmhPQXmPeOSi2R-gKx0ZAZeQKUi0ew7qwIsJIk130_assertion SIO_000772 14506070 NP235407.RANolmCmmhPQXmPeOSi2R-gKx0ZAZeQKUi0ew7qwIsJIk130_provenance.
- NP235407.RANolmCmmhPQXmPeOSi2R-gKx0ZAZeQKUi0ew7qwIsJIk130_assertion evidence source_evidence_literature NP235407.RANolmCmmhPQXmPeOSi2R-gKx0ZAZeQKUi0ew7qwIsJIk130_provenance.
- NP235407.RANolmCmmhPQXmPeOSi2R-gKx0ZAZeQKUi0ew7qwIsJIk130_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." NP235407.RANolmCmmhPQXmPeOSi2R-gKx0ZAZeQKUi0ew7qwIsJIk130_provenance.