Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP1066.RANLFnLRqwieb8_2DU53qnUzEU--g4jnockAVxNNsnT-0130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP1066.RANLFnLRqwieb8_2DU53qnUzEU--g4jnockAVxNNsnT-0130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP1066.RANLFnLRqwieb8_2DU53qnUzEU--g4jnockAVxNNsnT-0130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP1066.RANLFnLRqwieb8_2DU53qnUzEU--g4jnockAVxNNsnT-0130_provenance.
- NP1066.RANLFnLRqwieb8_2DU53qnUzEU--g4jnockAVxNNsnT-0130_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." NP1066.RANLFnLRqwieb8_2DU53qnUzEU--g4jnockAVxNNsnT-0130_provenance.
- NP1066.RANLFnLRqwieb8_2DU53qnUzEU--g4jnockAVxNNsnT-0130_assertion evidence source_evidence_curated NP1066.RANLFnLRqwieb8_2DU53qnUzEU--g4jnockAVxNNsnT-0130_provenance.
- NP1066.RANLFnLRqwieb8_2DU53qnUzEU--g4jnockAVxNNsnT-0130_assertion SIO_000772 14583443 NP1066.RANLFnLRqwieb8_2DU53qnUzEU--g4jnockAVxNNsnT-0130_provenance.
- NP1066.RANLFnLRqwieb8_2DU53qnUzEU--g4jnockAVxNNsnT-0130_assertion wasDerivedFrom uniprot-20130724 NP1066.RANLFnLRqwieb8_2DU53qnUzEU--g4jnockAVxNNsnT-0130_provenance.
- NP1066.RANLFnLRqwieb8_2DU53qnUzEU--g4jnockAVxNNsnT-0130_assertion wasGeneratedBy ECO_0000218 NP1066.RANLFnLRqwieb8_2DU53qnUzEU--g4jnockAVxNNsnT-0130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP1066.RANLFnLRqwieb8_2DU53qnUzEU--g4jnockAVxNNsnT-0130_provenance.