Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP826903.RA4RiGgS3ISVatxE9y6AVLYT4LBs8jgZHIXr3ynFkBcnY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP826903.RA4RiGgS3ISVatxE9y6AVLYT4LBs8jgZHIXr3ynFkBcnY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP826903.RA4RiGgS3ISVatxE9y6AVLYT4LBs8jgZHIXr3ynFkBcnY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP826903.RA4RiGgS3ISVatxE9y6AVLYT4LBs8jgZHIXr3ynFkBcnY130_provenance.
- NP826903.RA4RiGgS3ISVatxE9y6AVLYT4LBs8jgZHIXr3ynFkBcnY130_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." NP826903.RA4RiGgS3ISVatxE9y6AVLYT4LBs8jgZHIXr3ynFkBcnY130_provenance.
- NP826903.RA4RiGgS3ISVatxE9y6AVLYT4LBs8jgZHIXr3ynFkBcnY130_assertion evidence source_evidence_literature NP826903.RA4RiGgS3ISVatxE9y6AVLYT4LBs8jgZHIXr3ynFkBcnY130_provenance.
- NP826903.RA4RiGgS3ISVatxE9y6AVLYT4LBs8jgZHIXr3ynFkBcnY130_assertion SIO_000772 16979429 NP826903.RA4RiGgS3ISVatxE9y6AVLYT4LBs8jgZHIXr3ynFkBcnY130_provenance.
- NP826903.RA4RiGgS3ISVatxE9y6AVLYT4LBs8jgZHIXr3ynFkBcnY130_assertion wasDerivedFrom befree-20150227 NP826903.RA4RiGgS3ISVatxE9y6AVLYT4LBs8jgZHIXr3ynFkBcnY130_provenance.
- NP826903.RA4RiGgS3ISVatxE9y6AVLYT4LBs8jgZHIXr3ynFkBcnY130_assertion wasGeneratedBy ECO_0000203 NP826903.RA4RiGgS3ISVatxE9y6AVLYT4LBs8jgZHIXr3ynFkBcnY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP826903.RA4RiGgS3ISVatxE9y6AVLYT4LBs8jgZHIXr3ynFkBcnY130_provenance.