Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP791627.RALsVmuuH9elwxRX88l0bN8I7TzgsMfO6rhMqZB4VYwKo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP791627.RALsVmuuH9elwxRX88l0bN8I7TzgsMfO6rhMqZB4VYwKo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP791627.RALsVmuuH9elwxRX88l0bN8I7TzgsMfO6rhMqZB4VYwKo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP791627.RALsVmuuH9elwxRX88l0bN8I7TzgsMfO6rhMqZB4VYwKo130_provenance.
- NP791627.RALsVmuuH9elwxRX88l0bN8I7TzgsMfO6rhMqZB4VYwKo130_assertion description "[In contrast, rapid eye movement sleep behaviour disorder and hypocretin deficiency are rare in narcolepsy without cataplexy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP791627.RALsVmuuH9elwxRX88l0bN8I7TzgsMfO6rhMqZB4VYwKo130_provenance.
- NP791627.RALsVmuuH9elwxRX88l0bN8I7TzgsMfO6rhMqZB4VYwKo130_assertion evidence source_evidence_literature NP791627.RALsVmuuH9elwxRX88l0bN8I7TzgsMfO6rhMqZB4VYwKo130_provenance.
- NP791627.RALsVmuuH9elwxRX88l0bN8I7TzgsMfO6rhMqZB4VYwKo130_assertion SIO_000772 20129934 NP791627.RALsVmuuH9elwxRX88l0bN8I7TzgsMfO6rhMqZB4VYwKo130_provenance.
- NP791627.RALsVmuuH9elwxRX88l0bN8I7TzgsMfO6rhMqZB4VYwKo130_assertion wasDerivedFrom befree-2016 NP791627.RALsVmuuH9elwxRX88l0bN8I7TzgsMfO6rhMqZB4VYwKo130_provenance.
- NP791627.RALsVmuuH9elwxRX88l0bN8I7TzgsMfO6rhMqZB4VYwKo130_assertion wasGeneratedBy ECO_0000203 NP791627.RALsVmuuH9elwxRX88l0bN8I7TzgsMfO6rhMqZB4VYwKo130_provenance.
- befree-2016 importedOn "2016-02-19" NP791627.RALsVmuuH9elwxRX88l0bN8I7TzgsMfO6rhMqZB4VYwKo130_provenance.