Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP47154.RAxeyQN4nH0wFWvf4zLSi1U--kuEse19R6Fzr76g8dZIc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP47154.RAxeyQN4nH0wFWvf4zLSi1U--kuEse19R6Fzr76g8dZIc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP47154.RAxeyQN4nH0wFWvf4zLSi1U--kuEse19R6Fzr76g8dZIc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP47154.RAxeyQN4nH0wFWvf4zLSi1U--kuEse19R6Fzr76g8dZIc130_provenance.
- NP47154.RAxeyQN4nH0wFWvf4zLSi1U--kuEse19R6Fzr76g8dZIc130_assertion wasGeneratedBy ECO_0000203 NP47154.RAxeyQN4nH0wFWvf4zLSi1U--kuEse19R6Fzr76g8dZIc130_provenance.
- NP47154.RAxeyQN4nH0wFWvf4zLSi1U--kuEse19R6Fzr76g8dZIc130_assertion wasDerivedFrom gad-20130706 NP47154.RAxeyQN4nH0wFWvf4zLSi1U--kuEse19R6Fzr76g8dZIc130_provenance.
- NP47154.RAxeyQN4nH0wFWvf4zLSi1U--kuEse19R6Fzr76g8dZIc130_assertion SIO_000772 14739370 NP47154.RAxeyQN4nH0wFWvf4zLSi1U--kuEse19R6Fzr76g8dZIc130_provenance.
- NP47154.RAxeyQN4nH0wFWvf4zLSi1U--kuEse19R6Fzr76g8dZIc130_assertion evidence source_evidence_literature NP47154.RAxeyQN4nH0wFWvf4zLSi1U--kuEse19R6Fzr76g8dZIc130_provenance.
- NP47154.RAxeyQN4nH0wFWvf4zLSi1U--kuEse19R6Fzr76g8dZIc130_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." NP47154.RAxeyQN4nH0wFWvf4zLSi1U--kuEse19R6Fzr76g8dZIc130_provenance.
- gad-20130706 importedOn "2013-07-06" NP47154.RAxeyQN4nH0wFWvf4zLSi1U--kuEse19R6Fzr76g8dZIc130_provenance.