Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP6464.RAClbV-hhr7Y073ISWTpJBzx0IWgZ-brDlqTJq0yPBhso130_assertion> ?p ?o ?g. }
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- NP6464.RAClbV-hhr7Y073ISWTpJBzx0IWgZ-brDlqTJq0yPBhso130_assertion type Assertion NP6464.RAClbV-hhr7Y073ISWTpJBzx0IWgZ-brDlqTJq0yPBhso130_head.
- NP6464.RAClbV-hhr7Y073ISWTpJBzx0IWgZ-brDlqTJq0yPBhso130_assertion description "[CHARGE syndrome is an autosomal dominant multisystem disorder caused by mutation in the CHD7 gene, encoding chromodomain helicase DNA-binding protein 7.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP6464.RAClbV-hhr7Y073ISWTpJBzx0IWgZ-brDlqTJq0yPBhso130_provenance.
- NP6464.RAClbV-hhr7Y073ISWTpJBzx0IWgZ-brDlqTJq0yPBhso130_assertion evidence source_evidence_curated NP6464.RAClbV-hhr7Y073ISWTpJBzx0IWgZ-brDlqTJq0yPBhso130_provenance.
- NP6464.RAClbV-hhr7Y073ISWTpJBzx0IWgZ-brDlqTJq0yPBhso130_assertion SIO_000772 21158681 NP6464.RAClbV-hhr7Y073ISWTpJBzx0IWgZ-brDlqTJq0yPBhso130_provenance.
- NP6464.RAClbV-hhr7Y073ISWTpJBzx0IWgZ-brDlqTJq0yPBhso130_assertion wasDerivedFrom uniprot-2016 NP6464.RAClbV-hhr7Y073ISWTpJBzx0IWgZ-brDlqTJq0yPBhso130_provenance.
- NP6464.RAClbV-hhr7Y073ISWTpJBzx0IWgZ-brDlqTJq0yPBhso130_assertion wasGeneratedBy ECO_0000218 NP6464.RAClbV-hhr7Y073ISWTpJBzx0IWgZ-brDlqTJq0yPBhso130_provenance.