Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP56632.RA79E2vKJ3WsmEeIikQwhMBXNC7K7uZTSQwsI2-rmU3vE130_assertion> ?p ?o ?g. }
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- NP56632.RA79E2vKJ3WsmEeIikQwhMBXNC7K7uZTSQwsI2-rmU3vE130_assertion type Assertion NP56632.RA79E2vKJ3WsmEeIikQwhMBXNC7K7uZTSQwsI2-rmU3vE130_head.
- NP56632.RA79E2vKJ3WsmEeIikQwhMBXNC7K7uZTSQwsI2-rmU3vE130_assertion description "[Complement factor H mutations and gene polymorphisms in haemolytic uraemic syndrome: the C-257T, the A2089G and the G2881T polymorphisms are strongly associated with the disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP56632.RA79E2vKJ3WsmEeIikQwhMBXNC7K7uZTSQwsI2-rmU3vE130_provenance.
- NP56632.RA79E2vKJ3WsmEeIikQwhMBXNC7K7uZTSQwsI2-rmU3vE130_assertion evidence source_evidence_literature NP56632.RA79E2vKJ3WsmEeIikQwhMBXNC7K7uZTSQwsI2-rmU3vE130_provenance.
- NP56632.RA79E2vKJ3WsmEeIikQwhMBXNC7K7uZTSQwsI2-rmU3vE130_assertion SIO_000772 14583443 NP56632.RA79E2vKJ3WsmEeIikQwhMBXNC7K7uZTSQwsI2-rmU3vE130_provenance.
- NP56632.RA79E2vKJ3WsmEeIikQwhMBXNC7K7uZTSQwsI2-rmU3vE130_assertion wasDerivedFrom gad-20150221 NP56632.RA79E2vKJ3WsmEeIikQwhMBXNC7K7uZTSQwsI2-rmU3vE130_provenance.
- NP56632.RA79E2vKJ3WsmEeIikQwhMBXNC7K7uZTSQwsI2-rmU3vE130_assertion wasGeneratedBy ECO_0000203 NP56632.RA79E2vKJ3WsmEeIikQwhMBXNC7K7uZTSQwsI2-rmU3vE130_provenance.