Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP573851.RAsKwfNg_PLY2krXkYL5R1f0bxp4hxwOyrC47CXVVmTks130_assertion> ?p ?o ?g. }
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- NP573851.RAsKwfNg_PLY2krXkYL5R1f0bxp4hxwOyrC47CXVVmTks130_assertion type Assertion NP573851.RAsKwfNg_PLY2krXkYL5R1f0bxp4hxwOyrC47CXVVmTks130_head.
- NP573851.RAsKwfNg_PLY2krXkYL5R1f0bxp4hxwOyrC47CXVVmTks130_assertion wasGeneratedBy ECO_0000203 NP573851.RAsKwfNg_PLY2krXkYL5R1f0bxp4hxwOyrC47CXVVmTks130_provenance.
- NP573851.RAsKwfNg_PLY2krXkYL5R1f0bxp4hxwOyrC47CXVVmTks130_assertion wasDerivedFrom befree-20140225 NP573851.RAsKwfNg_PLY2krXkYL5R1f0bxp4hxwOyrC47CXVVmTks130_provenance.
- NP573851.RAsKwfNg_PLY2krXkYL5R1f0bxp4hxwOyrC47CXVVmTks130_assertion SIO_000772 23691182 NP573851.RAsKwfNg_PLY2krXkYL5R1f0bxp4hxwOyrC47CXVVmTks130_provenance.
- NP573851.RAsKwfNg_PLY2krXkYL5R1f0bxp4hxwOyrC47CXVVmTks130_assertion evidence source_evidence_literature NP573851.RAsKwfNg_PLY2krXkYL5R1f0bxp4hxwOyrC47CXVVmTks130_provenance.
- NP573851.RAsKwfNg_PLY2krXkYL5R1f0bxp4hxwOyrC47CXVVmTks130_assertion description "[The NOD2 SNP8 mutant was significantly more frequent in MM patients compared to controls (p = 0.0004, OR = 12.2, 95% CI = 2.6-57.8).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP573851.RAsKwfNg_PLY2krXkYL5R1f0bxp4hxwOyrC47CXVVmTks130_provenance.