Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP844600.RApgSmJn7H2IWiW5289ByQ2hpEJAcSZRRa8mfzY7fYo8U130_assertion> ?p ?o ?g. }
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- NP844600.RApgSmJn7H2IWiW5289ByQ2hpEJAcSZRRa8mfzY7fYo8U130_assertion type Assertion NP844600.RApgSmJn7H2IWiW5289ByQ2hpEJAcSZRRa8mfzY7fYo8U130_head.
- NP844600.RApgSmJn7H2IWiW5289ByQ2hpEJAcSZRRa8mfzY7fYo8U130_assertion description "[Large de novo deletion of 7p15.1 to 7p12.1 involving the imprinted gene GRB10 associated with a complex phenotype including features of Beckwith Wiedemann syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP844600.RApgSmJn7H2IWiW5289ByQ2hpEJAcSZRRa8mfzY7fYo8U130_provenance.
- NP844600.RApgSmJn7H2IWiW5289ByQ2hpEJAcSZRRa8mfzY7fYo8U130_assertion evidence source_evidence_literature NP844600.RApgSmJn7H2IWiW5289ByQ2hpEJAcSZRRa8mfzY7fYo8U130_provenance.
- NP844600.RApgSmJn7H2IWiW5289ByQ2hpEJAcSZRRa8mfzY7fYo8U130_assertion SIO_000772 20933618 NP844600.RApgSmJn7H2IWiW5289ByQ2hpEJAcSZRRa8mfzY7fYo8U130_provenance.
- NP844600.RApgSmJn7H2IWiW5289ByQ2hpEJAcSZRRa8mfzY7fYo8U130_assertion wasDerivedFrom befree-2016 NP844600.RApgSmJn7H2IWiW5289ByQ2hpEJAcSZRRa8mfzY7fYo8U130_provenance.
- NP844600.RApgSmJn7H2IWiW5289ByQ2hpEJAcSZRRa8mfzY7fYo8U130_assertion wasGeneratedBy ECO_0000203 NP844600.RApgSmJn7H2IWiW5289ByQ2hpEJAcSZRRa8mfzY7fYo8U130_provenance.