Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP269103.RAw_3AcbDyujM_JQK_VcHCWH26NQA-i5byK9VMc7QtxlA130_assertion> ?p ?o ?g. }
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- NP269103.RAw_3AcbDyujM_JQK_VcHCWH26NQA-i5byK9VMc7QtxlA130_assertion type Assertion NP269103.RAw_3AcbDyujM_JQK_VcHCWH26NQA-i5byK9VMc7QtxlA130_head.
- NP269103.RAw_3AcbDyujM_JQK_VcHCWH26NQA-i5byK9VMc7QtxlA130_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." NP269103.RAw_3AcbDyujM_JQK_VcHCWH26NQA-i5byK9VMc7QtxlA130_provenance.
- NP269103.RAw_3AcbDyujM_JQK_VcHCWH26NQA-i5byK9VMc7QtxlA130_assertion evidence source_evidence_literature NP269103.RAw_3AcbDyujM_JQK_VcHCWH26NQA-i5byK9VMc7QtxlA130_provenance.
- NP269103.RAw_3AcbDyujM_JQK_VcHCWH26NQA-i5byK9VMc7QtxlA130_assertion SIO_000772 18812404 NP269103.RAw_3AcbDyujM_JQK_VcHCWH26NQA-i5byK9VMc7QtxlA130_provenance.
- NP269103.RAw_3AcbDyujM_JQK_VcHCWH26NQA-i5byK9VMc7QtxlA130_assertion wasDerivedFrom befree-20150227 NP269103.RAw_3AcbDyujM_JQK_VcHCWH26NQA-i5byK9VMc7QtxlA130_provenance.
- NP269103.RAw_3AcbDyujM_JQK_VcHCWH26NQA-i5byK9VMc7QtxlA130_assertion wasGeneratedBy ECO_0000203 NP269103.RAw_3AcbDyujM_JQK_VcHCWH26NQA-i5byK9VMc7QtxlA130_provenance.