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- NP761707.RAOvhescSXQUUY2l1WhHt3XOlHZpjlVUY5Boxh_wb2N3Y130_assertion type Assertion NP761707.RAOvhescSXQUUY2l1WhHt3XOlHZpjlVUY5Boxh_wb2N3Y130_head.
- NP761707.RAOvhescSXQUUY2l1WhHt3XOlHZpjlVUY5Boxh_wb2N3Y130_assertion description "[This study identified a novel disease-causing mutation p.R187C in MIP in a Chinese cataract family, expanding the mutation spectrum of MIP causing congenital cataract.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP761707.RAOvhescSXQUUY2l1WhHt3XOlHZpjlVUY5Boxh_wb2N3Y130_provenance.
- NP761707.RAOvhescSXQUUY2l1WhHt3XOlHZpjlVUY5Boxh_wb2N3Y130_assertion evidence source_evidence_literature NP761707.RAOvhescSXQUUY2l1WhHt3XOlHZpjlVUY5Boxh_wb2N3Y130_provenance.
- NP761707.RAOvhescSXQUUY2l1WhHt3XOlHZpjlVUY5Boxh_wb2N3Y130_assertion SIO_000772 21245956 NP761707.RAOvhescSXQUUY2l1WhHt3XOlHZpjlVUY5Boxh_wb2N3Y130_provenance.
- NP761707.RAOvhescSXQUUY2l1WhHt3XOlHZpjlVUY5Boxh_wb2N3Y130_assertion wasDerivedFrom befree-20140225 NP761707.RAOvhescSXQUUY2l1WhHt3XOlHZpjlVUY5Boxh_wb2N3Y130_provenance.
- NP761707.RAOvhescSXQUUY2l1WhHt3XOlHZpjlVUY5Boxh_wb2N3Y130_assertion wasGeneratedBy ECO_0000203 NP761707.RAOvhescSXQUUY2l1WhHt3XOlHZpjlVUY5Boxh_wb2N3Y130_provenance.