Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP573851.RAsKwfNg_PLY2krXkYL5R1f0bxp4hxwOyrC47CXVVmTks130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP573851.RAsKwfNg_PLY2krXkYL5R1f0bxp4hxwOyrC47CXVVmTks130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP573851.RAsKwfNg_PLY2krXkYL5R1f0bxp4hxwOyrC47CXVVmTks130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP573851.RAsKwfNg_PLY2krXkYL5R1f0bxp4hxwOyrC47CXVVmTks130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP573851.RAsKwfNg_PLY2krXkYL5R1f0bxp4hxwOyrC47CXVVmTks130_provenance.