Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP806572.RALmbw2aKDSYNhk2a5Uvgqh_Jvb3Jpar8V8pw3ut8nWM4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP806572.RALmbw2aKDSYNhk2a5Uvgqh_Jvb3Jpar8V8pw3ut8nWM4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP806572.RALmbw2aKDSYNhk2a5Uvgqh_Jvb3Jpar8V8pw3ut8nWM4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP806572.RALmbw2aKDSYNhk2a5Uvgqh_Jvb3Jpar8V8pw3ut8nWM4130_provenance.
- NP806572.RALmbw2aKDSYNhk2a5Uvgqh_Jvb3Jpar8V8pw3ut8nWM4130_assertion description "[AOA1 is associated with oculomotor apraxia, severe sensorimotor neuropathy, choreiform movements, cognitive impairment, and cerebellar atrophy at an early age.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP806572.RALmbw2aKDSYNhk2a5Uvgqh_Jvb3Jpar8V8pw3ut8nWM4130_provenance.
- NP806572.RALmbw2aKDSYNhk2a5Uvgqh_Jvb3Jpar8V8pw3ut8nWM4130_assertion evidence source_evidence_literature NP806572.RALmbw2aKDSYNhk2a5Uvgqh_Jvb3Jpar8V8pw3ut8nWM4130_provenance.
- NP806572.RALmbw2aKDSYNhk2a5Uvgqh_Jvb3Jpar8V8pw3ut8nWM4130_assertion SIO_000772 16700949 NP806572.RALmbw2aKDSYNhk2a5Uvgqh_Jvb3Jpar8V8pw3ut8nWM4130_provenance.
- NP806572.RALmbw2aKDSYNhk2a5Uvgqh_Jvb3Jpar8V8pw3ut8nWM4130_assertion wasDerivedFrom befree-20140225 NP806572.RALmbw2aKDSYNhk2a5Uvgqh_Jvb3Jpar8V8pw3ut8nWM4130_provenance.
- NP806572.RALmbw2aKDSYNhk2a5Uvgqh_Jvb3Jpar8V8pw3ut8nWM4130_assertion wasGeneratedBy ECO_0000203 NP806572.RALmbw2aKDSYNhk2a5Uvgqh_Jvb3Jpar8V8pw3ut8nWM4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP806572.RALmbw2aKDSYNhk2a5Uvgqh_Jvb3Jpar8V8pw3ut8nWM4130_provenance.