Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP723967.RAGo0XU356vqDjpzQcBbi7lLL3B_4-ln43KI2yb4QuFrg130_assertion> ?p ?o ?g. }
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- NP723967.RAGo0XU356vqDjpzQcBbi7lLL3B_4-ln43KI2yb4QuFrg130_assertion type Assertion NP723967.RAGo0XU356vqDjpzQcBbi7lLL3B_4-ln43KI2yb4QuFrg130_head.
- NP723967.RAGo0XU356vqDjpzQcBbi7lLL3B_4-ln43KI2yb4QuFrg130_assertion description "[We report a novel missense mutation, p.V42M, in CRYGS associated with bilateral congenital cataract in a family of Indian origin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP723967.RAGo0XU356vqDjpzQcBbi7lLL3B_4-ln43KI2yb4QuFrg130_provenance.
- NP723967.RAGo0XU356vqDjpzQcBbi7lLL3B_4-ln43KI2yb4QuFrg130_assertion evidence source_evidence_literature NP723967.RAGo0XU356vqDjpzQcBbi7lLL3B_4-ln43KI2yb4QuFrg130_provenance.
- NP723967.RAGo0XU356vqDjpzQcBbi7lLL3B_4-ln43KI2yb4QuFrg130_assertion SIO_000772 19262743 NP723967.RAGo0XU356vqDjpzQcBbi7lLL3B_4-ln43KI2yb4QuFrg130_provenance.
- NP723967.RAGo0XU356vqDjpzQcBbi7lLL3B_4-ln43KI2yb4QuFrg130_assertion wasDerivedFrom befree-2016 NP723967.RAGo0XU356vqDjpzQcBbi7lLL3B_4-ln43KI2yb4QuFrg130_provenance.
- NP723967.RAGo0XU356vqDjpzQcBbi7lLL3B_4-ln43KI2yb4QuFrg130_assertion wasGeneratedBy ECO_0000203 NP723967.RAGo0XU356vqDjpzQcBbi7lLL3B_4-ln43KI2yb4QuFrg130_provenance.