Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP17358.RAxanxLRdjn5-SLsyjO1dBW1P-fxCvNe9plkLmvzWCu2c130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP17358.RAxanxLRdjn5-SLsyjO1dBW1P-fxCvNe9plkLmvzWCu2c130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP17358.RAxanxLRdjn5-SLsyjO1dBW1P-fxCvNe9plkLmvzWCu2c130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP17358.RAxanxLRdjn5-SLsyjO1dBW1P-fxCvNe9plkLmvzWCu2c130_provenance.
- NP17358.RAxanxLRdjn5-SLsyjO1dBW1P-fxCvNe9plkLmvzWCu2c130_assertion description "[The variant HNMT allele frequencies were slightly higher among patients with asthma [16.0%, 95% confidence interval (CI) 12.0-20.0] and among patients with rhinitis (13.2, 95% CI 10.3-16.1) as compared with healthy subjects (11.5 95% CI 8.9-14.1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP17358.RAxanxLRdjn5-SLsyjO1dBW1P-fxCvNe9plkLmvzWCu2c130_provenance.
- NP17358.RAxanxLRdjn5-SLsyjO1dBW1P-fxCvNe9plkLmvzWCu2c130_assertion evidence source_evidence_curated NP17358.RAxanxLRdjn5-SLsyjO1dBW1P-fxCvNe9plkLmvzWCu2c130_provenance.
- NP17358.RAxanxLRdjn5-SLsyjO1dBW1P-fxCvNe9plkLmvzWCu2c130_assertion SIO_000772 17651147 NP17358.RAxanxLRdjn5-SLsyjO1dBW1P-fxCvNe9plkLmvzWCu2c130_provenance.
- NP17358.RAxanxLRdjn5-SLsyjO1dBW1P-fxCvNe9plkLmvzWCu2c130_assertion wasDerivedFrom ctd_human-20150221 NP17358.RAxanxLRdjn5-SLsyjO1dBW1P-fxCvNe9plkLmvzWCu2c130_provenance.
- NP17358.RAxanxLRdjn5-SLsyjO1dBW1P-fxCvNe9plkLmvzWCu2c130_assertion wasGeneratedBy ECO_0000218 NP17358.RAxanxLRdjn5-SLsyjO1dBW1P-fxCvNe9plkLmvzWCu2c130_provenance.
- ctd_human-20150221 importedOn "2015-02-21" NP17358.RAxanxLRdjn5-SLsyjO1dBW1P-fxCvNe9plkLmvzWCu2c130_provenance.