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- source_evidence_literature type ECO_0000212 NP826958.RAFEYO4LTakJDw_WT0wwsghUDEo3mPolK8SMN-3CM2N98130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP826958.RAFEYO4LTakJDw_WT0wwsghUDEo3mPolK8SMN-3CM2N98130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP826958.RAFEYO4LTakJDw_WT0wwsghUDEo3mPolK8SMN-3CM2N98130_provenance.
- NP826958.RAFEYO4LTakJDw_WT0wwsghUDEo3mPolK8SMN-3CM2N98130_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." NP826958.RAFEYO4LTakJDw_WT0wwsghUDEo3mPolK8SMN-3CM2N98130_provenance.
- NP826958.RAFEYO4LTakJDw_WT0wwsghUDEo3mPolK8SMN-3CM2N98130_assertion evidence source_evidence_literature NP826958.RAFEYO4LTakJDw_WT0wwsghUDEo3mPolK8SMN-3CM2N98130_provenance.
- NP826958.RAFEYO4LTakJDw_WT0wwsghUDEo3mPolK8SMN-3CM2N98130_assertion SIO_000772 16979429 NP826958.RAFEYO4LTakJDw_WT0wwsghUDEo3mPolK8SMN-3CM2N98130_provenance.
- NP826958.RAFEYO4LTakJDw_WT0wwsghUDEo3mPolK8SMN-3CM2N98130_assertion wasDerivedFrom befree-20150227 NP826958.RAFEYO4LTakJDw_WT0wwsghUDEo3mPolK8SMN-3CM2N98130_provenance.
- NP826958.RAFEYO4LTakJDw_WT0wwsghUDEo3mPolK8SMN-3CM2N98130_assertion wasGeneratedBy ECO_0000203 NP826958.RAFEYO4LTakJDw_WT0wwsghUDEo3mPolK8SMN-3CM2N98130_provenance.
- befree-20150227 importedOn "2015-02-27" NP826958.RAFEYO4LTakJDw_WT0wwsghUDEo3mPolK8SMN-3CM2N98130_provenance.