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- NP561955.RANYYMGPx94_NNlurbXiJA9fSoU1MM1XbC98D8zANEmW4130_assertion type Assertion NP561955.RANYYMGPx94_NNlurbXiJA9fSoU1MM1XbC98D8zANEmW4130_head.
- NP561955.RANYYMGPx94_NNlurbXiJA9fSoU1MM1XbC98D8zANEmW4130_assertion wasGeneratedBy ECO_0000203 NP561955.RANYYMGPx94_NNlurbXiJA9fSoU1MM1XbC98D8zANEmW4130_provenance.
- NP561955.RANYYMGPx94_NNlurbXiJA9fSoU1MM1XbC98D8zANEmW4130_assertion wasDerivedFrom befree-2016 NP561955.RANYYMGPx94_NNlurbXiJA9fSoU1MM1XbC98D8zANEmW4130_provenance.
- NP561955.RANYYMGPx94_NNlurbXiJA9fSoU1MM1XbC98D8zANEmW4130_assertion SIO_000772 16876867 NP561955.RANYYMGPx94_NNlurbXiJA9fSoU1MM1XbC98D8zANEmW4130_provenance.
- NP561955.RANYYMGPx94_NNlurbXiJA9fSoU1MM1XbC98D8zANEmW4130_assertion evidence source_evidence_literature NP561955.RANYYMGPx94_NNlurbXiJA9fSoU1MM1XbC98D8zANEmW4130_provenance.
- NP561955.RANYYMGPx94_NNlurbXiJA9fSoU1MM1XbC98D8zANEmW4130_assertion description "[A novel PITX2 mutation and a polymorphism in a 5-generation family with Axenfeld-Rieger anomaly and coexisting Fuchs' endothelial dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP561955.RANYYMGPx94_NNlurbXiJA9fSoU1MM1XbC98D8zANEmW4130_provenance.