sub:provenance {
<
http://identifiers.org/wikipathways/WP4008_r110707>
dc:title "NO/cGMP/PKG mediated Neuroprotection"@en .
<
http://identifiers.org/wikipathways/WP4148_r110682>
dc:title "Splicing factor NOVA regulated synaptic proteins"@en .
<
http://identifiers.org/wikipathways/WP4222_r107160>
dc:title "Phosphodiesterases in neuronal function"@en .
<
http://identifiers.org/wikipathways/WP4223_r107655>
dc:title "Ras Signaling"@en .
<
http://identifiers.org/wikipathways/WP4312_r104287>
dc:title "Rett syndrome causing genes"@en .
<
http://identifiers.org/wikipathways/WP4453_r102018>
dc:title "Transcriptional Regulation by MECP2"@en .
<
http://identifiers.org/wikipathways/WP4549_r108088>
dc:title "Fragile X Syndrome "@en .
<
http://identifiers.org/wikipathways/WP4698_r110708>
dc:title "Vitamin D-sensitive calcium signaling in depression"@en .
<
http://identifiers.org/wikipathways/WP4875_r110312>
dc:title "Disruption of postsynaptic signalling by CNV"@en .
sub:assertion has-source: pmid:22510460 ,
pmid:24533017 ,
pmid:30705620 , <
http://identifiers.org/wikipathways/WP4008_r110707> , <
http://identifiers.org/wikipathways/WP4148_r110682> , <
http://identifiers.org/wikipathways/WP4222_r107160> , <
http://identifiers.org/wikipathways/WP4223_r107655> , <
http://identifiers.org/wikipathways/WP4312_r104287> , <
http://identifiers.org/wikipathways/WP4453_r102018> , <
http://identifiers.org/wikipathways/WP4549_r108088> , <
http://identifiers.org/wikipathways/WP4698_r110708> , <
http://identifiers.org/wikipathways/WP4875_r110312> .
}