Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP782197.RA3XbFyNd5eEP3s49CvE8x-FLgKe0CUBPEM8I7sYbdOZU130_assertion> ?p ?o ?g. }
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- NP782197.RA3XbFyNd5eEP3s49CvE8x-FLgKe0CUBPEM8I7sYbdOZU130_assertion type Assertion NP782197.RA3XbFyNd5eEP3s49CvE8x-FLgKe0CUBPEM8I7sYbdOZU130_head.
- NP782197.RA3XbFyNd5eEP3s49CvE8x-FLgKe0CUBPEM8I7sYbdOZU130_assertion description "[The aim of the present study was to clarify whether factor H mutations were involved in genetic predisposition to hemolytic uremic syndrome, by performing linkage and mutation studies in a large number of patients from those referred to the Italian Registry for Recurrent and Familial HUS/TTP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP782197.RA3XbFyNd5eEP3s49CvE8x-FLgKe0CUBPEM8I7sYbdOZU130_provenance.
- NP782197.RA3XbFyNd5eEP3s49CvE8x-FLgKe0CUBPEM8I7sYbdOZU130_assertion evidence source_evidence_literature NP782197.RA3XbFyNd5eEP3s49CvE8x-FLgKe0CUBPEM8I7sYbdOZU130_provenance.
- NP782197.RA3XbFyNd5eEP3s49CvE8x-FLgKe0CUBPEM8I7sYbdOZU130_assertion SIO_000772 11158219 NP782197.RA3XbFyNd5eEP3s49CvE8x-FLgKe0CUBPEM8I7sYbdOZU130_provenance.
- NP782197.RA3XbFyNd5eEP3s49CvE8x-FLgKe0CUBPEM8I7sYbdOZU130_assertion wasDerivedFrom befree-20150227 NP782197.RA3XbFyNd5eEP3s49CvE8x-FLgKe0CUBPEM8I7sYbdOZU130_provenance.
- NP782197.RA3XbFyNd5eEP3s49CvE8x-FLgKe0CUBPEM8I7sYbdOZU130_assertion wasGeneratedBy ECO_0000203 NP782197.RA3XbFyNd5eEP3s49CvE8x-FLgKe0CUBPEM8I7sYbdOZU130_provenance.