Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP694556.RAOGdus6lt3TO5jRDoPLW057i4Kk49ema4smIyyoQTFu8130_assertion> ?p ?o ?g. }
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- NP694556.RAOGdus6lt3TO5jRDoPLW057i4Kk49ema4smIyyoQTFu8130_assertion type Assertion NP694556.RAOGdus6lt3TO5jRDoPLW057i4Kk49ema4smIyyoQTFu8130_head.
- NP694556.RAOGdus6lt3TO5jRDoPLW057i4Kk49ema4smIyyoQTFu8130_assertion description "[Our findings demonstrate a novel genomic disorder characterised by deletion of BMP2 with variable cognitive deficits and dysmorphic features and show that individuals bearing microdeletions in 20p12.3 often present with WPW syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP694556.RAOGdus6lt3TO5jRDoPLW057i4Kk49ema4smIyyoQTFu8130_provenance.
- NP694556.RAOGdus6lt3TO5jRDoPLW057i4Kk49ema4smIyyoQTFu8130_assertion evidence source_evidence_literature NP694556.RAOGdus6lt3TO5jRDoPLW057i4Kk49ema4smIyyoQTFu8130_provenance.
- NP694556.RAOGdus6lt3TO5jRDoPLW057i4Kk49ema4smIyyoQTFu8130_assertion SIO_000772 18812404 NP694556.RAOGdus6lt3TO5jRDoPLW057i4Kk49ema4smIyyoQTFu8130_provenance.
- NP694556.RAOGdus6lt3TO5jRDoPLW057i4Kk49ema4smIyyoQTFu8130_assertion wasDerivedFrom befree-2016 NP694556.RAOGdus6lt3TO5jRDoPLW057i4Kk49ema4smIyyoQTFu8130_provenance.
- NP694556.RAOGdus6lt3TO5jRDoPLW057i4Kk49ema4smIyyoQTFu8130_assertion wasGeneratedBy ECO_0000203 NP694556.RAOGdus6lt3TO5jRDoPLW057i4Kk49ema4smIyyoQTFu8130_provenance.