Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP780585.RAWUhSbjemGdIZPF-K95zcRaqzqCwHL4ZTWxtf2AWLV1A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP780585.RAWUhSbjemGdIZPF-K95zcRaqzqCwHL4ZTWxtf2AWLV1A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP780585.RAWUhSbjemGdIZPF-K95zcRaqzqCwHL4ZTWxtf2AWLV1A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP780585.RAWUhSbjemGdIZPF-K95zcRaqzqCwHL4ZTWxtf2AWLV1A130_provenance.
- NP780585.RAWUhSbjemGdIZPF-K95zcRaqzqCwHL4ZTWxtf2AWLV1A130_assertion wasGeneratedBy ECO_0000203 NP780585.RAWUhSbjemGdIZPF-K95zcRaqzqCwHL4ZTWxtf2AWLV1A130_provenance.
- NP780585.RAWUhSbjemGdIZPF-K95zcRaqzqCwHL4ZTWxtf2AWLV1A130_assertion wasDerivedFrom befree-20140225 NP780585.RAWUhSbjemGdIZPF-K95zcRaqzqCwHL4ZTWxtf2AWLV1A130_provenance.
- NP780585.RAWUhSbjemGdIZPF-K95zcRaqzqCwHL4ZTWxtf2AWLV1A130_assertion SIO_000772 14739370 NP780585.RAWUhSbjemGdIZPF-K95zcRaqzqCwHL4ZTWxtf2AWLV1A130_provenance.
- NP780585.RAWUhSbjemGdIZPF-K95zcRaqzqCwHL4ZTWxtf2AWLV1A130_assertion evidence source_evidence_literature NP780585.RAWUhSbjemGdIZPF-K95zcRaqzqCwHL4ZTWxtf2AWLV1A130_provenance.
- NP780585.RAWUhSbjemGdIZPF-K95zcRaqzqCwHL4ZTWxtf2AWLV1A130_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." NP780585.RAWUhSbjemGdIZPF-K95zcRaqzqCwHL4ZTWxtf2AWLV1A130_provenance.
- befree-20140225 importedOn "2014-02-25" NP780585.RAWUhSbjemGdIZPF-K95zcRaqzqCwHL4ZTWxtf2AWLV1A130_provenance.