Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP257811.RAdi8NeyIu8-UL3wZ4WaqWTzyw23aisO7lyCDyJ4jAmEg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP257811.RAdi8NeyIu8-UL3wZ4WaqWTzyw23aisO7lyCDyJ4jAmEg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP257811.RAdi8NeyIu8-UL3wZ4WaqWTzyw23aisO7lyCDyJ4jAmEg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP257811.RAdi8NeyIu8-UL3wZ4WaqWTzyw23aisO7lyCDyJ4jAmEg130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP257811.RAdi8NeyIu8-UL3wZ4WaqWTzyw23aisO7lyCDyJ4jAmEg130_provenance.