Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP462540.RAQD3kGQMCnmk1Cu2aN3p91HM_3VH_BdurKRgWDoUXal4130_assertion> ?p ?o ?g. }
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- NP462540.RAQD3kGQMCnmk1Cu2aN3p91HM_3VH_BdurKRgWDoUXal4130_assertion type Assertion NP462540.RAQD3kGQMCnmk1Cu2aN3p91HM_3VH_BdurKRgWDoUXal4130_head.
- 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.