Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP56632.RA79E2vKJ3WsmEeIikQwhMBXNC7K7uZTSQwsI2-rmU3vE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP56632.RA79E2vKJ3WsmEeIikQwhMBXNC7K7uZTSQwsI2-rmU3vE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP56632.RA79E2vKJ3WsmEeIikQwhMBXNC7K7uZTSQwsI2-rmU3vE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP56632.RA79E2vKJ3WsmEeIikQwhMBXNC7K7uZTSQwsI2-rmU3vE130_provenance.
- 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.
- gad-20150221 importedOn "2015-02-21" NP56632.RA79E2vKJ3WsmEeIikQwhMBXNC7K7uZTSQwsI2-rmU3vE130_provenance.