Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP526156.RAuDDzcprFrjma5icrWTnR7KHfKFsRDIK5aFjNALiohH0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP526156.RAuDDzcprFrjma5icrWTnR7KHfKFsRDIK5aFjNALiohH0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP526156.RAuDDzcprFrjma5icrWTnR7KHfKFsRDIK5aFjNALiohH0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP526156.RAuDDzcprFrjma5icrWTnR7KHfKFsRDIK5aFjNALiohH0130_provenance.
- NP526156.RAuDDzcprFrjma5icrWTnR7KHfKFsRDIK5aFjNALiohH0130_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." NP526156.RAuDDzcprFrjma5icrWTnR7KHfKFsRDIK5aFjNALiohH0130_provenance.
- NP526156.RAuDDzcprFrjma5icrWTnR7KHfKFsRDIK5aFjNALiohH0130_assertion evidence source_evidence_literature NP526156.RAuDDzcprFrjma5icrWTnR7KHfKFsRDIK5aFjNALiohH0130_provenance.
- NP526156.RAuDDzcprFrjma5icrWTnR7KHfKFsRDIK5aFjNALiohH0130_assertion SIO_000772 16338760 NP526156.RAuDDzcprFrjma5icrWTnR7KHfKFsRDIK5aFjNALiohH0130_provenance.
- NP526156.RAuDDzcprFrjma5icrWTnR7KHfKFsRDIK5aFjNALiohH0130_assertion wasDerivedFrom befree-2016 NP526156.RAuDDzcprFrjma5icrWTnR7KHfKFsRDIK5aFjNALiohH0130_provenance.
- NP526156.RAuDDzcprFrjma5icrWTnR7KHfKFsRDIK5aFjNALiohH0130_assertion wasGeneratedBy ECO_0000203 NP526156.RAuDDzcprFrjma5icrWTnR7KHfKFsRDIK5aFjNALiohH0130_provenance.
- befree-2016 importedOn "2016-02-19" NP526156.RAuDDzcprFrjma5icrWTnR7KHfKFsRDIK5aFjNALiohH0130_provenance.