Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP418525.RACz-ZdtbZL908sRNXS7CqIAktWOnXl_HZapLsMNQA3Oc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP418525.RACz-ZdtbZL908sRNXS7CqIAktWOnXl_HZapLsMNQA3Oc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP418525.RACz-ZdtbZL908sRNXS7CqIAktWOnXl_HZapLsMNQA3Oc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP418525.RACz-ZdtbZL908sRNXS7CqIAktWOnXl_HZapLsMNQA3Oc130_provenance.
- NP418525.RACz-ZdtbZL908sRNXS7CqIAktWOnXl_HZapLsMNQA3Oc130_assertion description "[We analysed the complete HF1 in 101 patients with HUS, in 32 with thrombotic thrombocytopenic purpura (TTP) and in 106 controls to evaluate the frequency of HF1 mutations, the clinical outcome in mutation and non-mutation carriers and the role of HF1 polymorphisms in the predisposition to HUS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP418525.RACz-ZdtbZL908sRNXS7CqIAktWOnXl_HZapLsMNQA3Oc130_provenance.
- NP418525.RACz-ZdtbZL908sRNXS7CqIAktWOnXl_HZapLsMNQA3Oc130_assertion evidence source_evidence_literature NP418525.RACz-ZdtbZL908sRNXS7CqIAktWOnXl_HZapLsMNQA3Oc130_provenance.
- NP418525.RACz-ZdtbZL908sRNXS7CqIAktWOnXl_HZapLsMNQA3Oc130_assertion SIO_000772 14583443 NP418525.RACz-ZdtbZL908sRNXS7CqIAktWOnXl_HZapLsMNQA3Oc130_provenance.
- NP418525.RACz-ZdtbZL908sRNXS7CqIAktWOnXl_HZapLsMNQA3Oc130_assertion wasDerivedFrom befree-2016 NP418525.RACz-ZdtbZL908sRNXS7CqIAktWOnXl_HZapLsMNQA3Oc130_provenance.
- NP418525.RACz-ZdtbZL908sRNXS7CqIAktWOnXl_HZapLsMNQA3Oc130_assertion wasGeneratedBy ECO_0000203 NP418525.RACz-ZdtbZL908sRNXS7CqIAktWOnXl_HZapLsMNQA3Oc130_provenance.
- befree-2016 importedOn "2016-02-19" NP418525.RACz-ZdtbZL908sRNXS7CqIAktWOnXl_HZapLsMNQA3Oc130_provenance.