Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP269070.RAuvCwW9SoT_bx8IcvPv0_NHSIOX7sBodg47P70YJdpQk130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP269070.RAuvCwW9SoT_bx8IcvPv0_NHSIOX7sBodg47P70YJdpQk130_assertion type Assertion NP269070.RAuvCwW9SoT_bx8IcvPv0_NHSIOX7sBodg47P70YJdpQk130_head.
- NP269070.RAuvCwW9SoT_bx8IcvPv0_NHSIOX7sBodg47P70YJdpQk130_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." NP269070.RAuvCwW9SoT_bx8IcvPv0_NHSIOX7sBodg47P70YJdpQk130_provenance.
- NP269070.RAuvCwW9SoT_bx8IcvPv0_NHSIOX7sBodg47P70YJdpQk130_assertion evidence source_evidence_literature NP269070.RAuvCwW9SoT_bx8IcvPv0_NHSIOX7sBodg47P70YJdpQk130_provenance.
- NP269070.RAuvCwW9SoT_bx8IcvPv0_NHSIOX7sBodg47P70YJdpQk130_assertion SIO_000772 18812404 NP269070.RAuvCwW9SoT_bx8IcvPv0_NHSIOX7sBodg47P70YJdpQk130_provenance.
- NP269070.RAuvCwW9SoT_bx8IcvPv0_NHSIOX7sBodg47P70YJdpQk130_assertion wasDerivedFrom befree-20150227 NP269070.RAuvCwW9SoT_bx8IcvPv0_NHSIOX7sBodg47P70YJdpQk130_provenance.
- NP269070.RAuvCwW9SoT_bx8IcvPv0_NHSIOX7sBodg47P70YJdpQk130_assertion wasGeneratedBy ECO_0000203 NP269070.RAuvCwW9SoT_bx8IcvPv0_NHSIOX7sBodg47P70YJdpQk130_provenance.