Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1235248.RAEcXrHyagYVS7KMm7oX01H0QmQY7AhWtswzlp_AqnpBM130_assertion> ?p ?o ?g. }
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- NP1235248.RAEcXrHyagYVS7KMm7oX01H0QmQY7AhWtswzlp_AqnpBM130_assertion type Assertion NP1235248.RAEcXrHyagYVS7KMm7oX01H0QmQY7AhWtswzlp_AqnpBM130_head.
- NP1235248.RAEcXrHyagYVS7KMm7oX01H0QmQY7AhWtswzlp_AqnpBM130_assertion description "[We validated three SNPs (rs78142040, rs9605146 and rs3848719) in additional ARDS patients to substantiate their associations with susceptibility, severity and outcome of ARDS. rs78142040 (C>T) occurs within a histone mark (intron 6) of the Arylsulfatase D gene. rs9605146 (G>A) causes a deleterious coding change (proline to leucine) in the XK, Kell blood group complex subunit-related family, member 3 gene. rs3848719 (G>A) is a synonymous SNP in the Zinc-Finger/Leucine-Zipper Co-Transducer NIF1 gene. rs78142040, rs9605146, and rs3848719 are associated significantly with susceptibility to ARDS. rs3848719 is associated with APACHE II score quartile. rs78142040 is associated with 60-day mortality in the overall ARDS patient population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1235248.RAEcXrHyagYVS7KMm7oX01H0QmQY7AhWtswzlp_AqnpBM130_provenance.
- NP1235248.RAEcXrHyagYVS7KMm7oX01H0QmQY7AhWtswzlp_AqnpBM130_assertion evidence source_evidence_literature NP1235248.RAEcXrHyagYVS7KMm7oX01H0QmQY7AhWtswzlp_AqnpBM130_provenance.
- NP1235248.RAEcXrHyagYVS7KMm7oX01H0QmQY7AhWtswzlp_AqnpBM130_assertion SIO_000772 25372662 NP1235248.RAEcXrHyagYVS7KMm7oX01H0QmQY7AhWtswzlp_AqnpBM130_provenance.
- NP1235248.RAEcXrHyagYVS7KMm7oX01H0QmQY7AhWtswzlp_AqnpBM130_assertion wasDerivedFrom befree-2016 NP1235248.RAEcXrHyagYVS7KMm7oX01H0QmQY7AhWtswzlp_AqnpBM130_provenance.
- NP1235248.RAEcXrHyagYVS7KMm7oX01H0QmQY7AhWtswzlp_AqnpBM130_assertion wasGeneratedBy ECO_0000203 NP1235248.RAEcXrHyagYVS7KMm7oX01H0QmQY7AhWtswzlp_AqnpBM130_provenance.