Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP826903.RA4RiGgS3ISVatxE9y6AVLYT4LBs8jgZHIXr3ynFkBcnY130_assertion> ?p ?o ?g. }
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- NP826903.RA4RiGgS3ISVatxE9y6AVLYT4LBs8jgZHIXr3ynFkBcnY130_assertion type Assertion NP826903.RA4RiGgS3ISVatxE9y6AVLYT4LBs8jgZHIXr3ynFkBcnY130_head.
- 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.