Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP445144.RAKTBY8lx19PcFGjuIT2oXN_GDJBvHhHQbzAUt6g8E9dM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP445144.RAKTBY8lx19PcFGjuIT2oXN_GDJBvHhHQbzAUt6g8E9dM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP445144.RAKTBY8lx19PcFGjuIT2oXN_GDJBvHhHQbzAUt6g8E9dM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP445144.RAKTBY8lx19PcFGjuIT2oXN_GDJBvHhHQbzAUt6g8E9dM130_provenance.
- NP445144.RAKTBY8lx19PcFGjuIT2oXN_GDJBvHhHQbzAUt6g8E9dM130_assertion description "[The KLS patients had normal hypocretin levels while asymptomatic, but one KLS patient (also affected with Prader-Willi syndrome) showed a twofold decrease in hypocretin levels during a symptomatic episode.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP445144.RAKTBY8lx19PcFGjuIT2oXN_GDJBvHhHQbzAUt6g8E9dM130_provenance.
- NP445144.RAKTBY8lx19PcFGjuIT2oXN_GDJBvHhHQbzAUt6g8E9dM130_assertion evidence source_evidence_literature NP445144.RAKTBY8lx19PcFGjuIT2oXN_GDJBvHhHQbzAUt6g8E9dM130_provenance.
- NP445144.RAKTBY8lx19PcFGjuIT2oXN_GDJBvHhHQbzAUt6g8E9dM130_assertion SIO_000772 14638887 NP445144.RAKTBY8lx19PcFGjuIT2oXN_GDJBvHhHQbzAUt6g8E9dM130_provenance.
- NP445144.RAKTBY8lx19PcFGjuIT2oXN_GDJBvHhHQbzAUt6g8E9dM130_assertion wasDerivedFrom befree-20150227 NP445144.RAKTBY8lx19PcFGjuIT2oXN_GDJBvHhHQbzAUt6g8E9dM130_provenance.
- NP445144.RAKTBY8lx19PcFGjuIT2oXN_GDJBvHhHQbzAUt6g8E9dM130_assertion wasGeneratedBy ECO_0000203 NP445144.RAKTBY8lx19PcFGjuIT2oXN_GDJBvHhHQbzAUt6g8E9dM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP445144.RAKTBY8lx19PcFGjuIT2oXN_GDJBvHhHQbzAUt6g8E9dM130_provenance.