Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP160669.RAoRdqhjrSdn38wShzO9sRgxVAhtXwF1P7Fu2VQzPqLeA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP160669.RAoRdqhjrSdn38wShzO9sRgxVAhtXwF1P7Fu2VQzPqLeA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP160669.RAoRdqhjrSdn38wShzO9sRgxVAhtXwF1P7Fu2VQzPqLeA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP160669.RAoRdqhjrSdn38wShzO9sRgxVAhtXwF1P7Fu2VQzPqLeA130_provenance.
- 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.
- gad-20150221 importedOn "2015-02-21" NP160669.RAoRdqhjrSdn38wShzO9sRgxVAhtXwF1P7Fu2VQzPqLeA130_provenance.