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- NP71529.RAbVg5UIBAjXq6bdiXMa3ALcZjIRLmYI-xyKt1UcEwjxo130_assertion type Assertion NP71529.RAbVg5UIBAjXq6bdiXMa3ALcZjIRLmYI-xyKt1UcEwjxo130_head.
- 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.