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- source_evidence_literature type ECO_0000212 NP569612.RAe32KfHv9sfHhC58EpCDlCnO28MJh2auGfE-gw_odAg4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP569612.RAe32KfHv9sfHhC58EpCDlCnO28MJh2auGfE-gw_odAg4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP569612.RAe32KfHv9sfHhC58EpCDlCnO28MJh2auGfE-gw_odAg4130_provenance.
- NP569612.RAe32KfHv9sfHhC58EpCDlCnO28MJh2auGfE-gw_odAg4130_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." NP569612.RAe32KfHv9sfHhC58EpCDlCnO28MJh2auGfE-gw_odAg4130_provenance.
- NP569612.RAe32KfHv9sfHhC58EpCDlCnO28MJh2auGfE-gw_odAg4130_assertion evidence source_evidence_literature NP569612.RAe32KfHv9sfHhC58EpCDlCnO28MJh2auGfE-gw_odAg4130_provenance.
- NP569612.RAe32KfHv9sfHhC58EpCDlCnO28MJh2auGfE-gw_odAg4130_assertion SIO_000772 16979429 NP569612.RAe32KfHv9sfHhC58EpCDlCnO28MJh2auGfE-gw_odAg4130_provenance.
- NP569612.RAe32KfHv9sfHhC58EpCDlCnO28MJh2auGfE-gw_odAg4130_assertion wasDerivedFrom befree-2016 NP569612.RAe32KfHv9sfHhC58EpCDlCnO28MJh2auGfE-gw_odAg4130_provenance.
- NP569612.RAe32KfHv9sfHhC58EpCDlCnO28MJh2auGfE-gw_odAg4130_assertion wasGeneratedBy ECO_0000203 NP569612.RAe32KfHv9sfHhC58EpCDlCnO28MJh2auGfE-gw_odAg4130_provenance.
- befree-2016 importedOn "2016-02-19" NP569612.RAe32KfHv9sfHhC58EpCDlCnO28MJh2auGfE-gw_odAg4130_provenance.