Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP429226.RA5XOMB3BfVVANvP7ncSFIBi5RdGSjlXv0eCKgl5Auqjw130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP429226.RA5XOMB3BfVVANvP7ncSFIBi5RdGSjlXv0eCKgl5Auqjw130_assertion type Assertion NP429226.RA5XOMB3BfVVANvP7ncSFIBi5RdGSjlXv0eCKgl5Auqjw130_head.
- NP429226.RA5XOMB3BfVVANvP7ncSFIBi5RdGSjlXv0eCKgl5Auqjw130_assertion wasGeneratedBy ECO_0000203 NP429226.RA5XOMB3BfVVANvP7ncSFIBi5RdGSjlXv0eCKgl5Auqjw130_provenance.
- NP429226.RA5XOMB3BfVVANvP7ncSFIBi5RdGSjlXv0eCKgl5Auqjw130_assertion wasDerivedFrom befree-2016 NP429226.RA5XOMB3BfVVANvP7ncSFIBi5RdGSjlXv0eCKgl5Auqjw130_provenance.
- NP429226.RA5XOMB3BfVVANvP7ncSFIBi5RdGSjlXv0eCKgl5Auqjw130_assertion SIO_000772 14739370 NP429226.RA5XOMB3BfVVANvP7ncSFIBi5RdGSjlXv0eCKgl5Auqjw130_provenance.
- NP429226.RA5XOMB3BfVVANvP7ncSFIBi5RdGSjlXv0eCKgl5Auqjw130_assertion evidence source_evidence_literature NP429226.RA5XOMB3BfVVANvP7ncSFIBi5RdGSjlXv0eCKgl5Auqjw130_provenance.
- NP429226.RA5XOMB3BfVVANvP7ncSFIBi5RdGSjlXv0eCKgl5Auqjw130_assertion description "[We determined the -159T mutation of the CD14 gene, the 896G mutation of the toll-like receptor 4 gene, the 3020insC mutation of the NOD2 gene (NOD2-3020insC), the IL-6 174G/C promoter polymorphism (IL6-174G/C), and the mannose-binding lectin genotype and their association to the subsequent development of neonatal sepsis in a large cohort of very low birth weight (VLBW) infants.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP429226.RA5XOMB3BfVVANvP7ncSFIBi5RdGSjlXv0eCKgl5Auqjw130_provenance.