Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP682191.RASANS65Y7dHNYMqzFJkIijMGyIFzQuoNmh0hdql9VkQA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP682191.RASANS65Y7dHNYMqzFJkIijMGyIFzQuoNmh0hdql9VkQA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP682191.RASANS65Y7dHNYMqzFJkIijMGyIFzQuoNmh0hdql9VkQA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP682191.RASANS65Y7dHNYMqzFJkIijMGyIFzQuoNmh0hdql9VkQA130_provenance.
- NP682191.RASANS65Y7dHNYMqzFJkIijMGyIFzQuoNmh0hdql9VkQA130_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." NP682191.RASANS65Y7dHNYMqzFJkIijMGyIFzQuoNmh0hdql9VkQA130_provenance.
- NP682191.RASANS65Y7dHNYMqzFJkIijMGyIFzQuoNmh0hdql9VkQA130_assertion evidence source_evidence_literature NP682191.RASANS65Y7dHNYMqzFJkIijMGyIFzQuoNmh0hdql9VkQA130_provenance.
- NP682191.RASANS65Y7dHNYMqzFJkIijMGyIFzQuoNmh0hdql9VkQA130_assertion SIO_000772 17486179 NP682191.RASANS65Y7dHNYMqzFJkIijMGyIFzQuoNmh0hdql9VkQA130_provenance.
- NP682191.RASANS65Y7dHNYMqzFJkIijMGyIFzQuoNmh0hdql9VkQA130_assertion wasDerivedFrom befree-20140225 NP682191.RASANS65Y7dHNYMqzFJkIijMGyIFzQuoNmh0hdql9VkQA130_provenance.
- NP682191.RASANS65Y7dHNYMqzFJkIijMGyIFzQuoNmh0hdql9VkQA130_assertion wasGeneratedBy ECO_0000203 NP682191.RASANS65Y7dHNYMqzFJkIijMGyIFzQuoNmh0hdql9VkQA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP682191.RASANS65Y7dHNYMqzFJkIijMGyIFzQuoNmh0hdql9VkQA130_provenance.