Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP608743.RAwdr2DYvu0m745GqFORR8TmIdcTOexUN3KRAiuvITpRM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP608743.RAwdr2DYvu0m745GqFORR8TmIdcTOexUN3KRAiuvITpRM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP608743.RAwdr2DYvu0m745GqFORR8TmIdcTOexUN3KRAiuvITpRM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP608743.RAwdr2DYvu0m745GqFORR8TmIdcTOexUN3KRAiuvITpRM130_provenance.
- NP608743.RAwdr2DYvu0m745GqFORR8TmIdcTOexUN3KRAiuvITpRM130_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." NP608743.RAwdr2DYvu0m745GqFORR8TmIdcTOexUN3KRAiuvITpRM130_provenance.
- NP608743.RAwdr2DYvu0m745GqFORR8TmIdcTOexUN3KRAiuvITpRM130_assertion evidence source_evidence_literature NP608743.RAwdr2DYvu0m745GqFORR8TmIdcTOexUN3KRAiuvITpRM130_provenance.
- NP608743.RAwdr2DYvu0m745GqFORR8TmIdcTOexUN3KRAiuvITpRM130_assertion SIO_000772 17486179 NP608743.RAwdr2DYvu0m745GqFORR8TmIdcTOexUN3KRAiuvITpRM130_provenance.
- NP608743.RAwdr2DYvu0m745GqFORR8TmIdcTOexUN3KRAiuvITpRM130_assertion wasDerivedFrom befree-2016 NP608743.RAwdr2DYvu0m745GqFORR8TmIdcTOexUN3KRAiuvITpRM130_provenance.
- NP608743.RAwdr2DYvu0m745GqFORR8TmIdcTOexUN3KRAiuvITpRM130_assertion wasGeneratedBy ECO_0000203 NP608743.RAwdr2DYvu0m745GqFORR8TmIdcTOexUN3KRAiuvITpRM130_provenance.
- befree-2016 importedOn "2016-02-19" NP608743.RAwdr2DYvu0m745GqFORR8TmIdcTOexUN3KRAiuvITpRM130_provenance.