Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP867812.RAhBYume1om-ISO75Wj3GbDbNG6Kb4nbG9SMbciTB9hgQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP867812.RAhBYume1om-ISO75Wj3GbDbNG6Kb4nbG9SMbciTB9hgQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP867812.RAhBYume1om-ISO75Wj3GbDbNG6Kb4nbG9SMbciTB9hgQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP867812.RAhBYume1om-ISO75Wj3GbDbNG6Kb4nbG9SMbciTB9hgQ130_provenance.
- NP867812.RAhBYume1om-ISO75Wj3GbDbNG6Kb4nbG9SMbciTB9hgQ130_assertion description "[The phenotype was consistent with previous descriptions of AOA2, except for a higher frequency of strabism, and for the absence of oculomotor apraxia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP867812.RAhBYume1om-ISO75Wj3GbDbNG6Kb4nbG9SMbciTB9hgQ130_provenance.
- NP867812.RAhBYume1om-ISO75Wj3GbDbNG6Kb4nbG9SMbciTB9hgQ130_assertion evidence source_evidence_literature NP867812.RAhBYume1om-ISO75Wj3GbDbNG6Kb4nbG9SMbciTB9hgQ130_provenance.
- NP867812.RAhBYume1om-ISO75Wj3GbDbNG6Kb4nbG9SMbciTB9hgQ130_assertion SIO_000772 23941260 NP867812.RAhBYume1om-ISO75Wj3GbDbNG6Kb4nbG9SMbciTB9hgQ130_provenance.
- NP867812.RAhBYume1om-ISO75Wj3GbDbNG6Kb4nbG9SMbciTB9hgQ130_assertion wasDerivedFrom befree-20150227 NP867812.RAhBYume1om-ISO75Wj3GbDbNG6Kb4nbG9SMbciTB9hgQ130_provenance.
- NP867812.RAhBYume1om-ISO75Wj3GbDbNG6Kb4nbG9SMbciTB9hgQ130_assertion wasGeneratedBy ECO_0000203 NP867812.RAhBYume1om-ISO75Wj3GbDbNG6Kb4nbG9SMbciTB9hgQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP867812.RAhBYume1om-ISO75Wj3GbDbNG6Kb4nbG9SMbciTB9hgQ130_provenance.