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- source_evidence_literature type ECO_0000212 NP929668.RAcQ842jifabq-hV9I1oZocURit2AT_rLy1Nyz8N8w62o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP929668.RAcQ842jifabq-hV9I1oZocURit2AT_rLy1Nyz8N8w62o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP929668.RAcQ842jifabq-hV9I1oZocURit2AT_rLy1Nyz8N8w62o130_provenance.
- NP929668.RAcQ842jifabq-hV9I1oZocURit2AT_rLy1Nyz8N8w62o130_assertion description "[Rubinstein-Taybi syndrome (RSTS) is a congenital neurodevelopmental disorder defined by postnatal growth deficiency, characteristic skeletal abnormalities and mental retardation and caused by mutations in the genes encoding for the transcriptional co-activators with intrinsic lysine acetyltransferase (KAT) activity CBP and p300.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP929668.RAcQ842jifabq-hV9I1oZocURit2AT_rLy1Nyz8N8w62o130_provenance.
- NP929668.RAcQ842jifabq-hV9I1oZocURit2AT_rLy1Nyz8N8w62o130_assertion evidence source_evidence_literature NP929668.RAcQ842jifabq-hV9I1oZocURit2AT_rLy1Nyz8N8w62o130_provenance.
- NP929668.RAcQ842jifabq-hV9I1oZocURit2AT_rLy1Nyz8N8w62o130_assertion SIO_000772 21984751 NP929668.RAcQ842jifabq-hV9I1oZocURit2AT_rLy1Nyz8N8w62o130_provenance.
- NP929668.RAcQ842jifabq-hV9I1oZocURit2AT_rLy1Nyz8N8w62o130_assertion wasDerivedFrom befree-2016 NP929668.RAcQ842jifabq-hV9I1oZocURit2AT_rLy1Nyz8N8w62o130_provenance.
- NP929668.RAcQ842jifabq-hV9I1oZocURit2AT_rLy1Nyz8N8w62o130_assertion wasGeneratedBy ECO_0000203 NP929668.RAcQ842jifabq-hV9I1oZocURit2AT_rLy1Nyz8N8w62o130_provenance.
- befree-2016 importedOn "2016-02-19" NP929668.RAcQ842jifabq-hV9I1oZocURit2AT_rLy1Nyz8N8w62o130_provenance.