Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP298505.RAVLbpc0IM393wn9ggGlARwL_2PTS0_DZvX5Qjvvyvw-A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP298505.RAVLbpc0IM393wn9ggGlARwL_2PTS0_DZvX5Qjvvyvw-A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP298505.RAVLbpc0IM393wn9ggGlARwL_2PTS0_DZvX5Qjvvyvw-A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP298505.RAVLbpc0IM393wn9ggGlARwL_2PTS0_DZvX5Qjvvyvw-A130_provenance.
- NP298505.RAVLbpc0IM393wn9ggGlARwL_2PTS0_DZvX5Qjvvyvw-A130_assertion description "[A significant reduction in MeCP2 expression compared to age-matched controls was found in 11/14 autism (79%), 9/9 RTT (100%), 4/4 Angelman syndrome (100%), 3/4 Prader-Willi syndrome (75%), 3/5 Down syndrome (60%), and 2/2 attention deficit hyperactivity disorder (100%) frontal cortex samples.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP298505.RAVLbpc0IM393wn9ggGlARwL_2PTS0_DZvX5Qjvvyvw-A130_provenance.
- NP298505.RAVLbpc0IM393wn9ggGlARwL_2PTS0_DZvX5Qjvvyvw-A130_assertion evidence source_evidence_literature NP298505.RAVLbpc0IM393wn9ggGlARwL_2PTS0_DZvX5Qjvvyvw-A130_provenance.
- NP298505.RAVLbpc0IM393wn9ggGlARwL_2PTS0_DZvX5Qjvvyvw-A130_assertion SIO_000772 17486179 NP298505.RAVLbpc0IM393wn9ggGlARwL_2PTS0_DZvX5Qjvvyvw-A130_provenance.
- NP298505.RAVLbpc0IM393wn9ggGlARwL_2PTS0_DZvX5Qjvvyvw-A130_assertion wasDerivedFrom befree-20140225 NP298505.RAVLbpc0IM393wn9ggGlARwL_2PTS0_DZvX5Qjvvyvw-A130_provenance.
- NP298505.RAVLbpc0IM393wn9ggGlARwL_2PTS0_DZvX5Qjvvyvw-A130_assertion wasGeneratedBy ECO_0000203 NP298505.RAVLbpc0IM393wn9ggGlARwL_2PTS0_DZvX5Qjvvyvw-A130_provenance.
- befree-20140225 importedOn "2014-02-25" NP298505.RAVLbpc0IM393wn9ggGlARwL_2PTS0_DZvX5Qjvvyvw-A130_provenance.