Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP71529.RAbVg5UIBAjXq6bdiXMa3ALcZjIRLmYI-xyKt1UcEwjxo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP71529.RAbVg5UIBAjXq6bdiXMa3ALcZjIRLmYI-xyKt1UcEwjxo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP71529.RAbVg5UIBAjXq6bdiXMa3ALcZjIRLmYI-xyKt1UcEwjxo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP71529.RAbVg5UIBAjXq6bdiXMa3ALcZjIRLmYI-xyKt1UcEwjxo130_provenance.
- NP71529.RAbVg5UIBAjXq6bdiXMa3ALcZjIRLmYI-xyKt1UcEwjxo130_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." NP71529.RAbVg5UIBAjXq6bdiXMa3ALcZjIRLmYI-xyKt1UcEwjxo130_provenance.
- NP71529.RAbVg5UIBAjXq6bdiXMa3ALcZjIRLmYI-xyKt1UcEwjxo130_assertion evidence source_evidence_literature NP71529.RAbVg5UIBAjXq6bdiXMa3ALcZjIRLmYI-xyKt1UcEwjxo130_provenance.
- NP71529.RAbVg5UIBAjXq6bdiXMa3ALcZjIRLmYI-xyKt1UcEwjxo130_assertion SIO_000772 19948535 NP71529.RAbVg5UIBAjXq6bdiXMa3ALcZjIRLmYI-xyKt1UcEwjxo130_provenance.
- NP71529.RAbVg5UIBAjXq6bdiXMa3ALcZjIRLmYI-xyKt1UcEwjxo130_assertion wasDerivedFrom gad-20130706 NP71529.RAbVg5UIBAjXq6bdiXMa3ALcZjIRLmYI-xyKt1UcEwjxo130_provenance.
- NP71529.RAbVg5UIBAjXq6bdiXMa3ALcZjIRLmYI-xyKt1UcEwjxo130_assertion wasGeneratedBy ECO_0000203 NP71529.RAbVg5UIBAjXq6bdiXMa3ALcZjIRLmYI-xyKt1UcEwjxo130_provenance.
- gad-20130706 importedOn "2013-07-06" NP71529.RAbVg5UIBAjXq6bdiXMa3ALcZjIRLmYI-xyKt1UcEwjxo130_provenance.