Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP838217.RAtm565KSmrXGXnKVc1RpVnTxsEMAwLP-O6jtbDZfGbhY130_assertion> ?p ?o ?g. }
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- NP838217.RAtm565KSmrXGXnKVc1RpVnTxsEMAwLP-O6jtbDZfGbhY130_assertion type Assertion NP838217.RAtm565KSmrXGXnKVc1RpVnTxsEMAwLP-O6jtbDZfGbhY130_head.
- NP838217.RAtm565KSmrXGXnKVc1RpVnTxsEMAwLP-O6jtbDZfGbhY130_assertion description "[In humans, typing of the +1239A/C single nucleotide polymorphism (SNP) in the 3UTR of the Opn gene (SPP1) showed that +1239C carriers displayed higher Opn serum levels than +1239A homozygotes and a higher risk of developing autoimmune/lymphoproliferative syndrome, multiple sclerosis, and systemic lupus erythematosus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP838217.RAtm565KSmrXGXnKVc1RpVnTxsEMAwLP-O6jtbDZfGbhY130_provenance.
- NP838217.RAtm565KSmrXGXnKVc1RpVnTxsEMAwLP-O6jtbDZfGbhY130_assertion evidence source_evidence_literature NP838217.RAtm565KSmrXGXnKVc1RpVnTxsEMAwLP-O6jtbDZfGbhY130_provenance.
- NP838217.RAtm565KSmrXGXnKVc1RpVnTxsEMAwLP-O6jtbDZfGbhY130_assertion SIO_000772 20378012 NP838217.RAtm565KSmrXGXnKVc1RpVnTxsEMAwLP-O6jtbDZfGbhY130_provenance.
- NP838217.RAtm565KSmrXGXnKVc1RpVnTxsEMAwLP-O6jtbDZfGbhY130_assertion wasDerivedFrom befree-20140225 NP838217.RAtm565KSmrXGXnKVc1RpVnTxsEMAwLP-O6jtbDZfGbhY130_provenance.
- NP838217.RAtm565KSmrXGXnKVc1RpVnTxsEMAwLP-O6jtbDZfGbhY130_assertion wasGeneratedBy ECO_0000203 NP838217.RAtm565KSmrXGXnKVc1RpVnTxsEMAwLP-O6jtbDZfGbhY130_provenance.