Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP876998.RARI3YmvYH6EX1TTi74FmC3v_-s1ZNEDZOj9vUD9xeovc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP876998.RARI3YmvYH6EX1TTi74FmC3v_-s1ZNEDZOj9vUD9xeovc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP876998.RARI3YmvYH6EX1TTi74FmC3v_-s1ZNEDZOj9vUD9xeovc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP876998.RARI3YmvYH6EX1TTi74FmC3v_-s1ZNEDZOj9vUD9xeovc130_provenance.
- NP876998.RARI3YmvYH6EX1TTi74FmC3v_-s1ZNEDZOj9vUD9xeovc130_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." NP876998.RARI3YmvYH6EX1TTi74FmC3v_-s1ZNEDZOj9vUD9xeovc130_provenance.
- NP876998.RARI3YmvYH6EX1TTi74FmC3v_-s1ZNEDZOj9vUD9xeovc130_assertion evidence source_evidence_literature NP876998.RARI3YmvYH6EX1TTi74FmC3v_-s1ZNEDZOj9vUD9xeovc130_provenance.
- NP876998.RARI3YmvYH6EX1TTi74FmC3v_-s1ZNEDZOj9vUD9xeovc130_assertion SIO_000772 11158219 NP876998.RARI3YmvYH6EX1TTi74FmC3v_-s1ZNEDZOj9vUD9xeovc130_provenance.
- NP876998.RARI3YmvYH6EX1TTi74FmC3v_-s1ZNEDZOj9vUD9xeovc130_assertion wasDerivedFrom befree-20150227 NP876998.RARI3YmvYH6EX1TTi74FmC3v_-s1ZNEDZOj9vUD9xeovc130_provenance.
- NP876998.RARI3YmvYH6EX1TTi74FmC3v_-s1ZNEDZOj9vUD9xeovc130_assertion wasGeneratedBy ECO_0000203 NP876998.RARI3YmvYH6EX1TTi74FmC3v_-s1ZNEDZOj9vUD9xeovc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP876998.RARI3YmvYH6EX1TTi74FmC3v_-s1ZNEDZOj9vUD9xeovc130_provenance.