Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP585583.RAccnkvIFCQxP6JZsXDHzhh_LxZ9Z2gl9RUO15chKXcrU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP585583.RAccnkvIFCQxP6JZsXDHzhh_LxZ9Z2gl9RUO15chKXcrU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP585583.RAccnkvIFCQxP6JZsXDHzhh_LxZ9Z2gl9RUO15chKXcrU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP585583.RAccnkvIFCQxP6JZsXDHzhh_LxZ9Z2gl9RUO15chKXcrU130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP585583.RAccnkvIFCQxP6JZsXDHzhh_LxZ9Z2gl9RUO15chKXcrU130_provenance.