Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP844561.RAZEEWNJIOQYA-SGqHbRgWA3_9lel-zFs5sFjR3LIVzFU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP844561.RAZEEWNJIOQYA-SGqHbRgWA3_9lel-zFs5sFjR3LIVzFU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP844561.RAZEEWNJIOQYA-SGqHbRgWA3_9lel-zFs5sFjR3LIVzFU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP844561.RAZEEWNJIOQYA-SGqHbRgWA3_9lel-zFs5sFjR3LIVzFU130_provenance.
- NP844561.RAZEEWNJIOQYA-SGqHbRgWA3_9lel-zFs5sFjR3LIVzFU130_assertion description "[A de novo mutation in NKX2.5 associated with atrial septal defects, ventricular noncompaction, syncope and sudden death.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP844561.RAZEEWNJIOQYA-SGqHbRgWA3_9lel-zFs5sFjR3LIVzFU130_provenance.
- NP844561.RAZEEWNJIOQYA-SGqHbRgWA3_9lel-zFs5sFjR3LIVzFU130_assertion evidence source_evidence_literature NP844561.RAZEEWNJIOQYA-SGqHbRgWA3_9lel-zFs5sFjR3LIVzFU130_provenance.
- NP844561.RAZEEWNJIOQYA-SGqHbRgWA3_9lel-zFs5sFjR3LIVzFU130_assertion SIO_000772 20932824 NP844561.RAZEEWNJIOQYA-SGqHbRgWA3_9lel-zFs5sFjR3LIVzFU130_provenance.
- NP844561.RAZEEWNJIOQYA-SGqHbRgWA3_9lel-zFs5sFjR3LIVzFU130_assertion wasDerivedFrom befree-2016 NP844561.RAZEEWNJIOQYA-SGqHbRgWA3_9lel-zFs5sFjR3LIVzFU130_provenance.
- NP844561.RAZEEWNJIOQYA-SGqHbRgWA3_9lel-zFs5sFjR3LIVzFU130_assertion wasGeneratedBy ECO_0000203 NP844561.RAZEEWNJIOQYA-SGqHbRgWA3_9lel-zFs5sFjR3LIVzFU130_provenance.
- befree-2016 importedOn "2016-02-19" NP844561.RAZEEWNJIOQYA-SGqHbRgWA3_9lel-zFs5sFjR3LIVzFU130_provenance.