Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP490077.RA0y6qKX-98NuBJ3Lxjk5JuQ0-7U6dgaxy061mD3b4zYU130_assertion> ?p ?o ?g. }
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- NP490077.RA0y6qKX-98NuBJ3Lxjk5JuQ0-7U6dgaxy061mD3b4zYU130_assertion type Assertion NP490077.RA0y6qKX-98NuBJ3Lxjk5JuQ0-7U6dgaxy061mD3b4zYU130_head.
- NP490077.RA0y6qKX-98NuBJ3Lxjk5JuQ0-7U6dgaxy061mD3b4zYU130_assertion wasGeneratedBy ECO_0000203 NP490077.RA0y6qKX-98NuBJ3Lxjk5JuQ0-7U6dgaxy061mD3b4zYU130_provenance.
- NP490077.RA0y6qKX-98NuBJ3Lxjk5JuQ0-7U6dgaxy061mD3b4zYU130_assertion wasDerivedFrom befree-20140225 NP490077.RA0y6qKX-98NuBJ3Lxjk5JuQ0-7U6dgaxy061mD3b4zYU130_provenance.
- NP490077.RA0y6qKX-98NuBJ3Lxjk5JuQ0-7U6dgaxy061mD3b4zYU130_assertion SIO_000772 14506070 NP490077.RA0y6qKX-98NuBJ3Lxjk5JuQ0-7U6dgaxy061mD3b4zYU130_provenance.
- NP490077.RA0y6qKX-98NuBJ3Lxjk5JuQ0-7U6dgaxy061mD3b4zYU130_assertion evidence source_evidence_literature NP490077.RA0y6qKX-98NuBJ3Lxjk5JuQ0-7U6dgaxy061mD3b4zYU130_provenance.
- NP490077.RA0y6qKX-98NuBJ3Lxjk5JuQ0-7U6dgaxy061mD3b4zYU130_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." NP490077.RA0y6qKX-98NuBJ3Lxjk5JuQ0-7U6dgaxy061mD3b4zYU130_provenance.