Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP852962.RAit9Wk6Lv3HaCaFHS-O1xuLfQeB0NNtdXaBeoy3R73ms130_assertion> ?p ?o ?g. }
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- NP852962.RAit9Wk6Lv3HaCaFHS-O1xuLfQeB0NNtdXaBeoy3R73ms130_assertion type Assertion NP852962.RAit9Wk6Lv3HaCaFHS-O1xuLfQeB0NNtdXaBeoy3R73ms130_head.
- NP852962.RAit9Wk6Lv3HaCaFHS-O1xuLfQeB0NNtdXaBeoy3R73ms130_assertion description "[These genetic changes include haploinsufficiency of SETBP1 associated with intellectual disability and loss of expressive language and truncations of ZMYND11 in individuals with autism, aggression and complex neuropsychiatric features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP852962.RAit9Wk6Lv3HaCaFHS-O1xuLfQeB0NNtdXaBeoy3R73ms130_provenance.
- NP852962.RAit9Wk6Lv3HaCaFHS-O1xuLfQeB0NNtdXaBeoy3R73ms130_assertion evidence source_evidence_literature NP852962.RAit9Wk6Lv3HaCaFHS-O1xuLfQeB0NNtdXaBeoy3R73ms130_provenance.
- NP852962.RAit9Wk6Lv3HaCaFHS-O1xuLfQeB0NNtdXaBeoy3R73ms130_assertion SIO_000772 25217958 NP852962.RAit9Wk6Lv3HaCaFHS-O1xuLfQeB0NNtdXaBeoy3R73ms130_provenance.
- NP852962.RAit9Wk6Lv3HaCaFHS-O1xuLfQeB0NNtdXaBeoy3R73ms130_assertion wasDerivedFrom befree-20150227 NP852962.RAit9Wk6Lv3HaCaFHS-O1xuLfQeB0NNtdXaBeoy3R73ms130_provenance.
- NP852962.RAit9Wk6Lv3HaCaFHS-O1xuLfQeB0NNtdXaBeoy3R73ms130_assertion wasGeneratedBy ECO_0000203 NP852962.RAit9Wk6Lv3HaCaFHS-O1xuLfQeB0NNtdXaBeoy3R73ms130_provenance.