Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP257811.RAdi8NeyIu8-UL3wZ4WaqWTzyw23aisO7lyCDyJ4jAmEg130_assertion> ?p ?o ?g. }
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- NP257811.RAdi8NeyIu8-UL3wZ4WaqWTzyw23aisO7lyCDyJ4jAmEg130_assertion type Assertion NP257811.RAdi8NeyIu8-UL3wZ4WaqWTzyw23aisO7lyCDyJ4jAmEg130_head.
- NP257811.RAdi8NeyIu8-UL3wZ4WaqWTzyw23aisO7lyCDyJ4jAmEg130_assertion description "[The OR for AMD among heterozygous carriers of the CFH 402H variant was 3.6 (95% CI: 1.6-7.8) compared to those with the wildtype genotype, when adjusted for HTRA1 -625G>A genotypes (p=0.001).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP257811.RAdi8NeyIu8-UL3wZ4WaqWTzyw23aisO7lyCDyJ4jAmEg130_provenance.
- NP257811.RAdi8NeyIu8-UL3wZ4WaqWTzyw23aisO7lyCDyJ4jAmEg130_assertion evidence source_evidence_literature NP257811.RAdi8NeyIu8-UL3wZ4WaqWTzyw23aisO7lyCDyJ4jAmEg130_provenance.
- NP257811.RAdi8NeyIu8-UL3wZ4WaqWTzyw23aisO7lyCDyJ4jAmEg130_assertion SIO_000772 17679948 NP257811.RAdi8NeyIu8-UL3wZ4WaqWTzyw23aisO7lyCDyJ4jAmEg130_provenance.
- NP257811.RAdi8NeyIu8-UL3wZ4WaqWTzyw23aisO7lyCDyJ4jAmEg130_assertion wasDerivedFrom befree-20140225 NP257811.RAdi8NeyIu8-UL3wZ4WaqWTzyw23aisO7lyCDyJ4jAmEg130_provenance.
- NP257811.RAdi8NeyIu8-UL3wZ4WaqWTzyw23aisO7lyCDyJ4jAmEg130_assertion wasGeneratedBy ECO_0000203 NP257811.RAdi8NeyIu8-UL3wZ4WaqWTzyw23aisO7lyCDyJ4jAmEg130_provenance.