Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP914753.RABq0qxs5GDjn0zBW8ga6TEAax12rruQdj-BnigiyT7qo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP914753.RABq0qxs5GDjn0zBW8ga6TEAax12rruQdj-BnigiyT7qo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP914753.RABq0qxs5GDjn0zBW8ga6TEAax12rruQdj-BnigiyT7qo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP914753.RABq0qxs5GDjn0zBW8ga6TEAax12rruQdj-BnigiyT7qo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP914753.RABq0qxs5GDjn0zBW8ga6TEAax12rruQdj-BnigiyT7qo130_provenance.
- 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.