Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP212085.RA2S92tCm-krQAu_0y8K2KuGaWGaM_Ccy7R08pqg9CFOU130_assertion> ?p ?o ?g. }
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- NP212085.RA2S92tCm-krQAu_0y8K2KuGaWGaM_Ccy7R08pqg9CFOU130_assertion type Assertion NP212085.RA2S92tCm-krQAu_0y8K2KuGaWGaM_Ccy7R08pqg9CFOU130_head.
- NP212085.RA2S92tCm-krQAu_0y8K2KuGaWGaM_Ccy7R08pqg9CFOU130_assertion description "[Heterozygous R1215Q mutation is found in atypical hemolytic uremic syndrome, with incomplete penetrance of the disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP212085.RA2S92tCm-krQAu_0y8K2KuGaWGaM_Ccy7R08pqg9CFOU130_provenance.
- NP212085.RA2S92tCm-krQAu_0y8K2KuGaWGaM_Ccy7R08pqg9CFOU130_assertion evidence source_evidence_literature NP212085.RA2S92tCm-krQAu_0y8K2KuGaWGaM_Ccy7R08pqg9CFOU130_provenance.
- NP212085.RA2S92tCm-krQAu_0y8K2KuGaWGaM_Ccy7R08pqg9CFOU130_assertion SIO_000772 17973958 NP212085.RA2S92tCm-krQAu_0y8K2KuGaWGaM_Ccy7R08pqg9CFOU130_provenance.
- NP212085.RA2S92tCm-krQAu_0y8K2KuGaWGaM_Ccy7R08pqg9CFOU130_assertion wasDerivedFrom lhgdn-20090331 NP212085.RA2S92tCm-krQAu_0y8K2KuGaWGaM_Ccy7R08pqg9CFOU130_provenance.
- NP212085.RA2S92tCm-krQAu_0y8K2KuGaWGaM_Ccy7R08pqg9CFOU130_assertion wasGeneratedBy ECO_0000203 NP212085.RA2S92tCm-krQAu_0y8K2KuGaWGaM_Ccy7R08pqg9CFOU130_provenance.