Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1216370.RARoz8gYr2Bsmv9lgw15RuWFcu3UEFO1WTNcTfJ3q_XaE130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1216370.RARoz8gYr2Bsmv9lgw15RuWFcu3UEFO1WTNcTfJ3q_XaE130_assertion type Assertion NP1216370.RARoz8gYr2Bsmv9lgw15RuWFcu3UEFO1WTNcTfJ3q_XaE130_head.
- NP1216370.RARoz8gYr2Bsmv9lgw15RuWFcu3UEFO1WTNcTfJ3q_XaE130_assertion description "[A novel variant in TBX20 (p.D176N) identified by whole-exome sequencing in combination with a congenital heart disease related gene filter is associated with familial atrial septal defect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1216370.RARoz8gYr2Bsmv9lgw15RuWFcu3UEFO1WTNcTfJ3q_XaE130_provenance.
- NP1216370.RARoz8gYr2Bsmv9lgw15RuWFcu3UEFO1WTNcTfJ3q_XaE130_assertion evidence source_evidence_literature NP1216370.RARoz8gYr2Bsmv9lgw15RuWFcu3UEFO1WTNcTfJ3q_XaE130_provenance.
- NP1216370.RARoz8gYr2Bsmv9lgw15RuWFcu3UEFO1WTNcTfJ3q_XaE130_assertion SIO_000772 25183037 NP1216370.RARoz8gYr2Bsmv9lgw15RuWFcu3UEFO1WTNcTfJ3q_XaE130_provenance.
- NP1216370.RARoz8gYr2Bsmv9lgw15RuWFcu3UEFO1WTNcTfJ3q_XaE130_assertion wasDerivedFrom befree-2016 NP1216370.RARoz8gYr2Bsmv9lgw15RuWFcu3UEFO1WTNcTfJ3q_XaE130_provenance.
- NP1216370.RARoz8gYr2Bsmv9lgw15RuWFcu3UEFO1WTNcTfJ3q_XaE130_assertion wasGeneratedBy ECO_0000203 NP1216370.RARoz8gYr2Bsmv9lgw15RuWFcu3UEFO1WTNcTfJ3q_XaE130_provenance.