Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP809295.RAp_aCs7ng-GI_wEOaBHw6udYbCOL0V25mbzZk6GU2Mvc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP809295.RAp_aCs7ng-GI_wEOaBHw6udYbCOL0V25mbzZk6GU2Mvc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP809295.RAp_aCs7ng-GI_wEOaBHw6udYbCOL0V25mbzZk6GU2Mvc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP809295.RAp_aCs7ng-GI_wEOaBHw6udYbCOL0V25mbzZk6GU2Mvc130_provenance.
- NP809295.RAp_aCs7ng-GI_wEOaBHw6udYbCOL0V25mbzZk6GU2Mvc130_assertion description "[For instance, a point mutation in a human clock gene (Per2) was shown to produce the rare advanced sleep phase syndrome, whereas a functional polymorphism in Per3 is associated with the more frequent delayed sleep phase syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP809295.RAp_aCs7ng-GI_wEOaBHw6udYbCOL0V25mbzZk6GU2Mvc130_provenance.
- NP809295.RAp_aCs7ng-GI_wEOaBHw6udYbCOL0V25mbzZk6GU2Mvc130_assertion evidence source_evidence_literature NP809295.RAp_aCs7ng-GI_wEOaBHw6udYbCOL0V25mbzZk6GU2Mvc130_provenance.
- NP809295.RAp_aCs7ng-GI_wEOaBHw6udYbCOL0V25mbzZk6GU2Mvc130_assertion SIO_000772 16979429 NP809295.RAp_aCs7ng-GI_wEOaBHw6udYbCOL0V25mbzZk6GU2Mvc130_provenance.
- NP809295.RAp_aCs7ng-GI_wEOaBHw6udYbCOL0V25mbzZk6GU2Mvc130_assertion wasDerivedFrom befree-20150227 NP809295.RAp_aCs7ng-GI_wEOaBHw6udYbCOL0V25mbzZk6GU2Mvc130_provenance.
- NP809295.RAp_aCs7ng-GI_wEOaBHw6udYbCOL0V25mbzZk6GU2Mvc130_assertion wasGeneratedBy ECO_0000203 NP809295.RAp_aCs7ng-GI_wEOaBHw6udYbCOL0V25mbzZk6GU2Mvc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP809295.RAp_aCs7ng-GI_wEOaBHw6udYbCOL0V25mbzZk6GU2Mvc130_provenance.