Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP116407.RAw_OcZ3Q9AEs0Y6YeMXPfDfOy7xVjk9EyBIn8bD0gycA130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP116407.RAw_OcZ3Q9AEs0Y6YeMXPfDfOy7xVjk9EyBIn8bD0gycA130_assertion type Assertion NP116407.RAw_OcZ3Q9AEs0Y6YeMXPfDfOy7xVjk9EyBIn8bD0gycA130_head.
- NP116407.RAw_OcZ3Q9AEs0Y6YeMXPfDfOy7xVjk9EyBIn8bD0gycA130_assertion description "[Compared to PLEKHA1, HTRA1/LOC387715 genetic variations were independently and strongly associated with exudative AMD in the French population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP116407.RAw_OcZ3Q9AEs0Y6YeMXPfDfOy7xVjk9EyBIn8bD0gycA130_provenance.
- NP116407.RAw_OcZ3Q9AEs0Y6YeMXPfDfOy7xVjk9EyBIn8bD0gycA130_assertion evidence source_evidence_literature NP116407.RAw_OcZ3Q9AEs0Y6YeMXPfDfOy7xVjk9EyBIn8bD0gycA130_provenance.
- NP116407.RAw_OcZ3Q9AEs0Y6YeMXPfDfOy7xVjk9EyBIn8bD0gycA130_assertion SIO_000772 18079691 NP116407.RAw_OcZ3Q9AEs0Y6YeMXPfDfOy7xVjk9EyBIn8bD0gycA130_provenance.
- NP116407.RAw_OcZ3Q9AEs0Y6YeMXPfDfOy7xVjk9EyBIn8bD0gycA130_assertion wasDerivedFrom gad-20150221 NP116407.RAw_OcZ3Q9AEs0Y6YeMXPfDfOy7xVjk9EyBIn8bD0gycA130_provenance.
- NP116407.RAw_OcZ3Q9AEs0Y6YeMXPfDfOy7xVjk9EyBIn8bD0gycA130_assertion wasGeneratedBy ECO_0000203 NP116407.RAw_OcZ3Q9AEs0Y6YeMXPfDfOy7xVjk9EyBIn8bD0gycA130_provenance.