Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP886740.RAxPDb6PIvilYTFLB-pf4CuWFHxpLM92JElDqkElvfJEE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP886740.RAxPDb6PIvilYTFLB-pf4CuWFHxpLM92JElDqkElvfJEE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP886740.RAxPDb6PIvilYTFLB-pf4CuWFHxpLM92JElDqkElvfJEE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP886740.RAxPDb6PIvilYTFLB-pf4CuWFHxpLM92JElDqkElvfJEE130_provenance.
- NP886740.RAxPDb6PIvilYTFLB-pf4CuWFHxpLM92JElDqkElvfJEE130_assertion description "[The insertion/deletion polymorphism of the angiotensin-converting enzyme (ACE-ins/del) and the angiotensin II type 1 receptor 1166A/C polymorphism (ATR1166A/C) were reported to be associated with several unfavorable outcome parameters in preterm infants like bronchopulmonary dysplasia, persistent ductus arteriosus and impaired insulin sensitivity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP886740.RAxPDb6PIvilYTFLB-pf4CuWFHxpLM92JElDqkElvfJEE130_provenance.
- NP886740.RAxPDb6PIvilYTFLB-pf4CuWFHxpLM92JElDqkElvfJEE130_assertion evidence source_evidence_literature NP886740.RAxPDb6PIvilYTFLB-pf4CuWFHxpLM92JElDqkElvfJEE130_provenance.
- NP886740.RAxPDb6PIvilYTFLB-pf4CuWFHxpLM92JElDqkElvfJEE130_assertion SIO_000772 19571582 NP886740.RAxPDb6PIvilYTFLB-pf4CuWFHxpLM92JElDqkElvfJEE130_provenance.
- NP886740.RAxPDb6PIvilYTFLB-pf4CuWFHxpLM92JElDqkElvfJEE130_assertion wasDerivedFrom befree-20140225 NP886740.RAxPDb6PIvilYTFLB-pf4CuWFHxpLM92JElDqkElvfJEE130_provenance.
- NP886740.RAxPDb6PIvilYTFLB-pf4CuWFHxpLM92JElDqkElvfJEE130_assertion wasGeneratedBy ECO_0000203 NP886740.RAxPDb6PIvilYTFLB-pf4CuWFHxpLM92JElDqkElvfJEE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP886740.RAxPDb6PIvilYTFLB-pf4CuWFHxpLM92JElDqkElvfJEE130_provenance.