Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP359575.RAwIsfhP1WqWazKedAU_BJhoqj6ZAPUUNFGXY9XWGvQYs130_assertion> ?p ?o ?g. }
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- NP359575.RAwIsfhP1WqWazKedAU_BJhoqj6ZAPUUNFGXY9XWGvQYs130_assertion type Assertion NP359575.RAwIsfhP1WqWazKedAU_BJhoqj6ZAPUUNFGXY9XWGvQYs130_head.
- NP359575.RAwIsfhP1WqWazKedAU_BJhoqj6ZAPUUNFGXY9XWGvQYs130_assertion description "[De novo mutations in SYNGAP1, which codes for a RAS/RAP GTP-activating protein, cause nonsyndromic intellectual disability (NSID).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP359575.RAwIsfhP1WqWazKedAU_BJhoqj6ZAPUUNFGXY9XWGvQYs130_provenance.
- NP359575.RAwIsfhP1WqWazKedAU_BJhoqj6ZAPUUNFGXY9XWGvQYs130_assertion evidence source_evidence_literature NP359575.RAwIsfhP1WqWazKedAU_BJhoqj6ZAPUUNFGXY9XWGvQYs130_provenance.
- NP359575.RAwIsfhP1WqWazKedAU_BJhoqj6ZAPUUNFGXY9XWGvQYs130_assertion SIO_000772 23161826 NP359575.RAwIsfhP1WqWazKedAU_BJhoqj6ZAPUUNFGXY9XWGvQYs130_provenance.
- NP359575.RAwIsfhP1WqWazKedAU_BJhoqj6ZAPUUNFGXY9XWGvQYs130_assertion wasDerivedFrom befree-20140225 NP359575.RAwIsfhP1WqWazKedAU_BJhoqj6ZAPUUNFGXY9XWGvQYs130_provenance.
- NP359575.RAwIsfhP1WqWazKedAU_BJhoqj6ZAPUUNFGXY9XWGvQYs130_assertion wasGeneratedBy ECO_0000203 NP359575.RAwIsfhP1WqWazKedAU_BJhoqj6ZAPUUNFGXY9XWGvQYs130_provenance.