Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP414209.RArGB-lmyAlhfKKvSVL3lq48fjqsxJp0yfIESPdqKGPb8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP414209.RArGB-lmyAlhfKKvSVL3lq48fjqsxJp0yfIESPdqKGPb8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP414209.RArGB-lmyAlhfKKvSVL3lq48fjqsxJp0yfIESPdqKGPb8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP414209.RArGB-lmyAlhfKKvSVL3lq48fjqsxJp0yfIESPdqKGPb8130_provenance.
- befree-2016 importedOn "2016-02-19" NP414209.RArGB-lmyAlhfKKvSVL3lq48fjqsxJp0yfIESPdqKGPb8130_provenance.
- NP414209.RArGB-lmyAlhfKKvSVL3lq48fjqsxJp0yfIESPdqKGPb8130_assertion wasGeneratedBy ECO_0000203 NP414209.RArGB-lmyAlhfKKvSVL3lq48fjqsxJp0yfIESPdqKGPb8130_provenance.
- NP414209.RArGB-lmyAlhfKKvSVL3lq48fjqsxJp0yfIESPdqKGPb8130_assertion wasDerivedFrom befree-2016 NP414209.RArGB-lmyAlhfKKvSVL3lq48fjqsxJp0yfIESPdqKGPb8130_provenance.
- NP414209.RArGB-lmyAlhfKKvSVL3lq48fjqsxJp0yfIESPdqKGPb8130_assertion SIO_000772 14506070 NP414209.RArGB-lmyAlhfKKvSVL3lq48fjqsxJp0yfIESPdqKGPb8130_provenance.
- NP414209.RArGB-lmyAlhfKKvSVL3lq48fjqsxJp0yfIESPdqKGPb8130_assertion evidence source_evidence_literature NP414209.RArGB-lmyAlhfKKvSVL3lq48fjqsxJp0yfIESPdqKGPb8130_provenance.
- NP414209.RArGB-lmyAlhfKKvSVL3lq48fjqsxJp0yfIESPdqKGPb8130_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." NP414209.RArGB-lmyAlhfKKvSVL3lq48fjqsxJp0yfIESPdqKGPb8130_provenance.