Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP1066.RANLFnLRqwieb8_2DU53qnUzEU--g4jnockAVxNNsnT-0130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1066.RANLFnLRqwieb8_2DU53qnUzEU--g4jnockAVxNNsnT-0130_assertion type Assertion NP1066.RANLFnLRqwieb8_2DU53qnUzEU--g4jnockAVxNNsnT-0130_head.
- 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.