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- source_evidence_literature type ECO_0000212 NP772417.RAwEwEVmyW7GOPJ6hxDu0FzN54_sU_l28XPe7sdm3H4hY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP772417.RAwEwEVmyW7GOPJ6hxDu0FzN54_sU_l28XPe7sdm3H4hY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP772417.RAwEwEVmyW7GOPJ6hxDu0FzN54_sU_l28XPe7sdm3H4hY130_provenance.
- NP772417.RAwEwEVmyW7GOPJ6hxDu0FzN54_sU_l28XPe7sdm3H4hY130_assertion description "[Although there were no pathogenic mutations in DLG4/PSD95 or GABARAP in a cohort study with 142 patients with idiopathic developmental delay with/without epilepsy, further studies would be required for genes included in this region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP772417.RAwEwEVmyW7GOPJ6hxDu0FzN54_sU_l28XPe7sdm3H4hY130_provenance.
- NP772417.RAwEwEVmyW7GOPJ6hxDu0FzN54_sU_l28XPe7sdm3H4hY130_assertion evidence source_evidence_literature NP772417.RAwEwEVmyW7GOPJ6hxDu0FzN54_sU_l28XPe7sdm3H4hY130_provenance.
- NP772417.RAwEwEVmyW7GOPJ6hxDu0FzN54_sU_l28XPe7sdm3H4hY130_assertion SIO_000772 20111057 NP772417.RAwEwEVmyW7GOPJ6hxDu0FzN54_sU_l28XPe7sdm3H4hY130_provenance.
- NP772417.RAwEwEVmyW7GOPJ6hxDu0FzN54_sU_l28XPe7sdm3H4hY130_assertion wasDerivedFrom befree-20140225 NP772417.RAwEwEVmyW7GOPJ6hxDu0FzN54_sU_l28XPe7sdm3H4hY130_provenance.
- NP772417.RAwEwEVmyW7GOPJ6hxDu0FzN54_sU_l28XPe7sdm3H4hY130_assertion wasGeneratedBy ECO_0000203 NP772417.RAwEwEVmyW7GOPJ6hxDu0FzN54_sU_l28XPe7sdm3H4hY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP772417.RAwEwEVmyW7GOPJ6hxDu0FzN54_sU_l28XPe7sdm3H4hY130_provenance.