Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP803897.RATH61fgiZd8zkI9zFBR50F-pnsgG6IAbyvIffTlC45Ic130_assertion> ?p ?o ?g. }
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- NP803897.RATH61fgiZd8zkI9zFBR50F-pnsgG6IAbyvIffTlC45Ic130_assertion type Assertion NP803897.RATH61fgiZd8zkI9zFBR50F-pnsgG6IAbyvIffTlC45Ic130_head.
- NP803897.RATH61fgiZd8zkI9zFBR50F-pnsgG6IAbyvIffTlC45Ic130_assertion description "[Notably, KS may also be part of pleiotropic developmental diseases including CHARGE syndrome; this disease results in most cases from neomutations in CHD7 that encodes a chromodomain helicase DNA-binding protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP803897.RATH61fgiZd8zkI9zFBR50F-pnsgG6IAbyvIffTlC45Ic130_provenance.
- NP803897.RATH61fgiZd8zkI9zFBR50F-pnsgG6IAbyvIffTlC45Ic130_assertion evidence source_evidence_literature NP803897.RATH61fgiZd8zkI9zFBR50F-pnsgG6IAbyvIffTlC45Ic130_provenance.
- NP803897.RATH61fgiZd8zkI9zFBR50F-pnsgG6IAbyvIffTlC45Ic130_assertion SIO_000772 20362962 NP803897.RATH61fgiZd8zkI9zFBR50F-pnsgG6IAbyvIffTlC45Ic130_provenance.
- NP803897.RATH61fgiZd8zkI9zFBR50F-pnsgG6IAbyvIffTlC45Ic130_assertion wasDerivedFrom befree-2016 NP803897.RATH61fgiZd8zkI9zFBR50F-pnsgG6IAbyvIffTlC45Ic130_provenance.
- NP803897.RATH61fgiZd8zkI9zFBR50F-pnsgG6IAbyvIffTlC45Ic130_assertion wasGeneratedBy ECO_0000203 NP803897.RATH61fgiZd8zkI9zFBR50F-pnsgG6IAbyvIffTlC45Ic130_provenance.