Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP285164.RAb61kKMIMdFGaxcxB7vioclgFES0WBs8xDc-_hslN6Wg130_assertion> ?p ?o ?g. }
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- NP285164.RAb61kKMIMdFGaxcxB7vioclgFES0WBs8xDc-_hslN6Wg130_assertion type Assertion NP285164.RAb61kKMIMdFGaxcxB7vioclgFES0WBs8xDc-_hslN6Wg130_head.
- NP285164.RAb61kKMIMdFGaxcxB7vioclgFES0WBs8xDc-_hslN6Wg130_assertion description "[To report two Japanese patients who were clinically diagnosed with late-onset and sporadic lattice corneal dystrophy (LCD) in whom a Leu527Arg mutation in the TGFBI gene was found.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP285164.RAb61kKMIMdFGaxcxB7vioclgFES0WBs8xDc-_hslN6Wg130_provenance.
- NP285164.RAb61kKMIMdFGaxcxB7vioclgFES0WBs8xDc-_hslN6Wg130_assertion evidence source_evidence_literature NP285164.RAb61kKMIMdFGaxcxB7vioclgFES0WBs8xDc-_hslN6Wg130_provenance.
- NP285164.RAb61kKMIMdFGaxcxB7vioclgFES0WBs8xDc-_hslN6Wg130_assertion SIO_000772 11413411 NP285164.RAb61kKMIMdFGaxcxB7vioclgFES0WBs8xDc-_hslN6Wg130_provenance.
- NP285164.RAb61kKMIMdFGaxcxB7vioclgFES0WBs8xDc-_hslN6Wg130_assertion wasDerivedFrom befree-20140225 NP285164.RAb61kKMIMdFGaxcxB7vioclgFES0WBs8xDc-_hslN6Wg130_provenance.
- NP285164.RAb61kKMIMdFGaxcxB7vioclgFES0WBs8xDc-_hslN6Wg130_assertion wasGeneratedBy ECO_0000203 NP285164.RAb61kKMIMdFGaxcxB7vioclgFES0WBs8xDc-_hslN6Wg130_provenance.