Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP599532.RAQsV-sCvebH2i7qXDCADai5JOcNC5dUB8K4g3EfUeuis130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP599532.RAQsV-sCvebH2i7qXDCADai5JOcNC5dUB8K4g3EfUeuis130_assertion type Assertion NP599532.RAQsV-sCvebH2i7qXDCADai5JOcNC5dUB8K4g3EfUeuis130_head.
- NP599532.RAQsV-sCvebH2i7qXDCADai5JOcNC5dUB8K4g3EfUeuis130_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." NP599532.RAQsV-sCvebH2i7qXDCADai5JOcNC5dUB8K4g3EfUeuis130_provenance.
- NP599532.RAQsV-sCvebH2i7qXDCADai5JOcNC5dUB8K4g3EfUeuis130_assertion evidence source_evidence_literature NP599532.RAQsV-sCvebH2i7qXDCADai5JOcNC5dUB8K4g3EfUeuis130_provenance.
- NP599532.RAQsV-sCvebH2i7qXDCADai5JOcNC5dUB8K4g3EfUeuis130_assertion SIO_000772 18812404 NP599532.RAQsV-sCvebH2i7qXDCADai5JOcNC5dUB8K4g3EfUeuis130_provenance.
- NP599532.RAQsV-sCvebH2i7qXDCADai5JOcNC5dUB8K4g3EfUeuis130_assertion wasDerivedFrom befree-20140225 NP599532.RAQsV-sCvebH2i7qXDCADai5JOcNC5dUB8K4g3EfUeuis130_provenance.
- NP599532.RAQsV-sCvebH2i7qXDCADai5JOcNC5dUB8K4g3EfUeuis130_assertion wasGeneratedBy ECO_0000203 NP599532.RAQsV-sCvebH2i7qXDCADai5JOcNC5dUB8K4g3EfUeuis130_provenance.