Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP484746.RA4DFUWkbr0Z6WA1pI-jleR0Prxn1o6ec-y09HTzd2bns130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP484746.RA4DFUWkbr0Z6WA1pI-jleR0Prxn1o6ec-y09HTzd2bns130_assertion type Assertion NP484746.RA4DFUWkbr0Z6WA1pI-jleR0Prxn1o6ec-y09HTzd2bns130_head.
- NP484746.RA4DFUWkbr0Z6WA1pI-jleR0Prxn1o6ec-y09HTzd2bns130_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." NP484746.RA4DFUWkbr0Z6WA1pI-jleR0Prxn1o6ec-y09HTzd2bns130_provenance.
- NP484746.RA4DFUWkbr0Z6WA1pI-jleR0Prxn1o6ec-y09HTzd2bns130_assertion evidence source_evidence_literature NP484746.RA4DFUWkbr0Z6WA1pI-jleR0Prxn1o6ec-y09HTzd2bns130_provenance.
- NP484746.RA4DFUWkbr0Z6WA1pI-jleR0Prxn1o6ec-y09HTzd2bns130_assertion SIO_000772 20378012 NP484746.RA4DFUWkbr0Z6WA1pI-jleR0Prxn1o6ec-y09HTzd2bns130_provenance.
- NP484746.RA4DFUWkbr0Z6WA1pI-jleR0Prxn1o6ec-y09HTzd2bns130_assertion wasDerivedFrom befree-20140225 NP484746.RA4DFUWkbr0Z6WA1pI-jleR0Prxn1o6ec-y09HTzd2bns130_provenance.
- NP484746.RA4DFUWkbr0Z6WA1pI-jleR0Prxn1o6ec-y09HTzd2bns130_assertion wasGeneratedBy ECO_0000203 NP484746.RA4DFUWkbr0Z6WA1pI-jleR0Prxn1o6ec-y09HTzd2bns130_provenance.