Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP160669.RAoRdqhjrSdn38wShzO9sRgxVAhtXwF1P7Fu2VQzPqLeA130_assertion> ?p ?o ?g. }
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- NP160669.RAoRdqhjrSdn38wShzO9sRgxVAhtXwF1P7Fu2VQzPqLeA130_assertion type Assertion NP160669.RAoRdqhjrSdn38wShzO9sRgxVAhtXwF1P7Fu2VQzPqLeA130_head.
- NP160669.RAoRdqhjrSdn38wShzO9sRgxVAhtXwF1P7Fu2VQzPqLeA130_assertion description "[Mutations in JAG1 were detected in three patients with Alagille syndrome (1.3%), while NKX2.5 mutations were seen in two patients with non-syndromic ToF (0.9%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP160669.RAoRdqhjrSdn38wShzO9sRgxVAhtXwF1P7Fu2VQzPqLeA130_provenance.
- NP160669.RAoRdqhjrSdn38wShzO9sRgxVAhtXwF1P7Fu2VQzPqLeA130_assertion evidence source_evidence_literature NP160669.RAoRdqhjrSdn38wShzO9sRgxVAhtXwF1P7Fu2VQzPqLeA130_provenance.
- NP160669.RAoRdqhjrSdn38wShzO9sRgxVAhtXwF1P7Fu2VQzPqLeA130_assertion SIO_000772 19948535 NP160669.RAoRdqhjrSdn38wShzO9sRgxVAhtXwF1P7Fu2VQzPqLeA130_provenance.
- NP160669.RAoRdqhjrSdn38wShzO9sRgxVAhtXwF1P7Fu2VQzPqLeA130_assertion wasDerivedFrom gad-20150221 NP160669.RAoRdqhjrSdn38wShzO9sRgxVAhtXwF1P7Fu2VQzPqLeA130_provenance.
- NP160669.RAoRdqhjrSdn38wShzO9sRgxVAhtXwF1P7Fu2VQzPqLeA130_assertion wasGeneratedBy ECO_0000203 NP160669.RAoRdqhjrSdn38wShzO9sRgxVAhtXwF1P7Fu2VQzPqLeA130_provenance.