Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP419466.RAN8tQ22AICHPp-ClbVN4mpUhdMEOL9cx4zSGrbhGFK1o130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP419466.RAN8tQ22AICHPp-ClbVN4mpUhdMEOL9cx4zSGrbhGFK1o130_assertion type Assertion NP419466.RAN8tQ22AICHPp-ClbVN4mpUhdMEOL9cx4zSGrbhGFK1o130_head.
- NP419466.RAN8tQ22AICHPp-ClbVN4mpUhdMEOL9cx4zSGrbhGFK1o130_assertion wasGeneratedBy ECO_0000203 NP419466.RAN8tQ22AICHPp-ClbVN4mpUhdMEOL9cx4zSGrbhGFK1o130_provenance.
- NP419466.RAN8tQ22AICHPp-ClbVN4mpUhdMEOL9cx4zSGrbhGFK1o130_assertion wasDerivedFrom befree-20150227 NP419466.RAN8tQ22AICHPp-ClbVN4mpUhdMEOL9cx4zSGrbhGFK1o130_provenance.
- NP419466.RAN8tQ22AICHPp-ClbVN4mpUhdMEOL9cx4zSGrbhGFK1o130_assertion SIO_000772 18055909 NP419466.RAN8tQ22AICHPp-ClbVN4mpUhdMEOL9cx4zSGrbhGFK1o130_provenance.
- NP419466.RAN8tQ22AICHPp-ClbVN4mpUhdMEOL9cx4zSGrbhGFK1o130_assertion evidence source_evidence_literature NP419466.RAN8tQ22AICHPp-ClbVN4mpUhdMEOL9cx4zSGrbhGFK1o130_provenance.
- NP419466.RAN8tQ22AICHPp-ClbVN4mpUhdMEOL9cx4zSGrbhGFK1o130_assertion description "[These data suggest that non-synonymous GATA4 sequence variants are found in a small percentage of patients with septal defects and are very uncommonly found in patients with conotruncal defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP419466.RAN8tQ22AICHPp-ClbVN4mpUhdMEOL9cx4zSGrbhGFK1o130_provenance.