Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP861218.RAMpjKiGVAxxjNPmTQPZ2GG_Az5zMLr3NEWj1LFP1oN5s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP861218.RAMpjKiGVAxxjNPmTQPZ2GG_Az5zMLr3NEWj1LFP1oN5s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP861218.RAMpjKiGVAxxjNPmTQPZ2GG_Az5zMLr3NEWj1LFP1oN5s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP861218.RAMpjKiGVAxxjNPmTQPZ2GG_Az5zMLr3NEWj1LFP1oN5s130_provenance.
- NP861218.RAMpjKiGVAxxjNPmTQPZ2GG_Az5zMLr3NEWj1LFP1oN5s130_assertion description "[Point mutations in the prion protein, period 2, and the prepro-hypocretin/orexin gene have been found as the cause of a few sleep disorders but the possibility that other gene defects may contribute to the pathophysiology of major sleep disorders is worth in-depth investigations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP861218.RAMpjKiGVAxxjNPmTQPZ2GG_Az5zMLr3NEWj1LFP1oN5s130_provenance.
- NP861218.RAMpjKiGVAxxjNPmTQPZ2GG_Az5zMLr3NEWj1LFP1oN5s130_assertion evidence source_evidence_literature NP861218.RAMpjKiGVAxxjNPmTQPZ2GG_Az5zMLr3NEWj1LFP1oN5s130_provenance.
- NP861218.RAMpjKiGVAxxjNPmTQPZ2GG_Az5zMLr3NEWj1LFP1oN5s130_assertion SIO_000772 16338760 NP861218.RAMpjKiGVAxxjNPmTQPZ2GG_Az5zMLr3NEWj1LFP1oN5s130_provenance.
- NP861218.RAMpjKiGVAxxjNPmTQPZ2GG_Az5zMLr3NEWj1LFP1oN5s130_assertion wasDerivedFrom befree-20140225 NP861218.RAMpjKiGVAxxjNPmTQPZ2GG_Az5zMLr3NEWj1LFP1oN5s130_provenance.
- NP861218.RAMpjKiGVAxxjNPmTQPZ2GG_Az5zMLr3NEWj1LFP1oN5s130_assertion wasGeneratedBy ECO_0000203 NP861218.RAMpjKiGVAxxjNPmTQPZ2GG_Az5zMLr3NEWj1LFP1oN5s130_provenance.
- befree-20140225 importedOn "2014-02-25" NP861218.RAMpjKiGVAxxjNPmTQPZ2GG_Az5zMLr3NEWj1LFP1oN5s130_provenance.