Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP462540.RAQD3kGQMCnmk1Cu2aN3p91HM_3VH_BdurKRgWDoUXal4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP462540.RAQD3kGQMCnmk1Cu2aN3p91HM_3VH_BdurKRgWDoUXal4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP462540.RAQD3kGQMCnmk1Cu2aN3p91HM_3VH_BdurKRgWDoUXal4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP462540.RAQD3kGQMCnmk1Cu2aN3p91HM_3VH_BdurKRgWDoUXal4130_provenance.
- NP462540.RAQD3kGQMCnmk1Cu2aN3p91HM_3VH_BdurKRgWDoUXal4130_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." NP462540.RAQD3kGQMCnmk1Cu2aN3p91HM_3VH_BdurKRgWDoUXal4130_provenance.
- NP462540.RAQD3kGQMCnmk1Cu2aN3p91HM_3VH_BdurKRgWDoUXal4130_assertion evidence source_evidence_literature NP462540.RAQD3kGQMCnmk1Cu2aN3p91HM_3VH_BdurKRgWDoUXal4130_provenance.
- NP462540.RAQD3kGQMCnmk1Cu2aN3p91HM_3VH_BdurKRgWDoUXal4130_assertion SIO_000772 20111057 NP462540.RAQD3kGQMCnmk1Cu2aN3p91HM_3VH_BdurKRgWDoUXal4130_provenance.
- NP462540.RAQD3kGQMCnmk1Cu2aN3p91HM_3VH_BdurKRgWDoUXal4130_assertion wasDerivedFrom befree-20140225 NP462540.RAQD3kGQMCnmk1Cu2aN3p91HM_3VH_BdurKRgWDoUXal4130_provenance.
- NP462540.RAQD3kGQMCnmk1Cu2aN3p91HM_3VH_BdurKRgWDoUXal4130_assertion wasGeneratedBy ECO_0000203 NP462540.RAQD3kGQMCnmk1Cu2aN3p91HM_3VH_BdurKRgWDoUXal4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP462540.RAQD3kGQMCnmk1Cu2aN3p91HM_3VH_BdurKRgWDoUXal4130_provenance.