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- source_evidence_literature type ECO_0000212 NP305468.RAlyDVi_VIAqsoKQ0zONvdQNs7zcqnHdwj6LWhO-T2xHA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP305468.RAlyDVi_VIAqsoKQ0zONvdQNs7zcqnHdwj6LWhO-T2xHA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP305468.RAlyDVi_VIAqsoKQ0zONvdQNs7zcqnHdwj6LWhO-T2xHA130_provenance.
- NP305468.RAlyDVi_VIAqsoKQ0zONvdQNs7zcqnHdwj6LWhO-T2xHA130_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." NP305468.RAlyDVi_VIAqsoKQ0zONvdQNs7zcqnHdwj6LWhO-T2xHA130_provenance.
- NP305468.RAlyDVi_VIAqsoKQ0zONvdQNs7zcqnHdwj6LWhO-T2xHA130_assertion evidence source_evidence_literature NP305468.RAlyDVi_VIAqsoKQ0zONvdQNs7zcqnHdwj6LWhO-T2xHA130_provenance.
- NP305468.RAlyDVi_VIAqsoKQ0zONvdQNs7zcqnHdwj6LWhO-T2xHA130_assertion SIO_000772 11158219 NP305468.RAlyDVi_VIAqsoKQ0zONvdQNs7zcqnHdwj6LWhO-T2xHA130_provenance.
- NP305468.RAlyDVi_VIAqsoKQ0zONvdQNs7zcqnHdwj6LWhO-T2xHA130_assertion wasDerivedFrom befree-2016 NP305468.RAlyDVi_VIAqsoKQ0zONvdQNs7zcqnHdwj6LWhO-T2xHA130_provenance.
- NP305468.RAlyDVi_VIAqsoKQ0zONvdQNs7zcqnHdwj6LWhO-T2xHA130_assertion wasGeneratedBy ECO_0000203 NP305468.RAlyDVi_VIAqsoKQ0zONvdQNs7zcqnHdwj6LWhO-T2xHA130_provenance.
- befree-2016 importedOn "2016-02-19" NP305468.RAlyDVi_VIAqsoKQ0zONvdQNs7zcqnHdwj6LWhO-T2xHA130_provenance.