Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP585583.RAccnkvIFCQxP6JZsXDHzhh_LxZ9Z2gl9RUO15chKXcrU130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP585583.RAccnkvIFCQxP6JZsXDHzhh_LxZ9Z2gl9RUO15chKXcrU130_assertion type Assertion NP585583.RAccnkvIFCQxP6JZsXDHzhh_LxZ9Z2gl9RUO15chKXcrU130_head.
- NP585583.RAccnkvIFCQxP6JZsXDHzhh_LxZ9Z2gl9RUO15chKXcrU130_assertion description "[Novel point mutation in the NKX2-5 gene in a Moroccan family with atrioventricular conduction disturbance and an atrial septal defect in the oval fossa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP585583.RAccnkvIFCQxP6JZsXDHzhh_LxZ9Z2gl9RUO15chKXcrU130_provenance.
- NP585583.RAccnkvIFCQxP6JZsXDHzhh_LxZ9Z2gl9RUO15chKXcrU130_assertion evidence source_evidence_literature NP585583.RAccnkvIFCQxP6JZsXDHzhh_LxZ9Z2gl9RUO15chKXcrU130_provenance.
- NP585583.RAccnkvIFCQxP6JZsXDHzhh_LxZ9Z2gl9RUO15chKXcrU130_assertion SIO_000772 17184575 NP585583.RAccnkvIFCQxP6JZsXDHzhh_LxZ9Z2gl9RUO15chKXcrU130_provenance.
- NP585583.RAccnkvIFCQxP6JZsXDHzhh_LxZ9Z2gl9RUO15chKXcrU130_assertion wasDerivedFrom befree-2016 NP585583.RAccnkvIFCQxP6JZsXDHzhh_LxZ9Z2gl9RUO15chKXcrU130_provenance.
- NP585583.RAccnkvIFCQxP6JZsXDHzhh_LxZ9Z2gl9RUO15chKXcrU130_assertion wasGeneratedBy ECO_0000203 NP585583.RAccnkvIFCQxP6JZsXDHzhh_LxZ9Z2gl9RUO15chKXcrU130_provenance.