Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP56163.RAtYRR4JS6bdqj9itImUItp2cgiRhCgPzo8hIhDqCeaTM130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP56163.RAtYRR4JS6bdqj9itImUItp2cgiRhCgPzo8hIhDqCeaTM130_assertion type Assertion NP56163.RAtYRR4JS6bdqj9itImUItp2cgiRhCgPzo8hIhDqCeaTM130_head.
- NP56163.RAtYRR4JS6bdqj9itImUItp2cgiRhCgPzo8hIhDqCeaTM130_assertion description "[Therefore, CST3 B may be a recessive risk allele, significantly contributing to disease risk in up to 6.6% of German ARMD patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP56163.RAtYRR4JS6bdqj9itImUItp2cgiRhCgPzo8hIhDqCeaTM130_provenance.
- NP56163.RAtYRR4JS6bdqj9itImUItp2cgiRhCgPzo8hIhDqCeaTM130_assertion evidence source_evidence_literature NP56163.RAtYRR4JS6bdqj9itImUItp2cgiRhCgPzo8hIhDqCeaTM130_provenance.
- NP56163.RAtYRR4JS6bdqj9itImUItp2cgiRhCgPzo8hIhDqCeaTM130_assertion SIO_000772 11815350 NP56163.RAtYRR4JS6bdqj9itImUItp2cgiRhCgPzo8hIhDqCeaTM130_provenance.
- NP56163.RAtYRR4JS6bdqj9itImUItp2cgiRhCgPzo8hIhDqCeaTM130_assertion wasDerivedFrom gad-20150221 NP56163.RAtYRR4JS6bdqj9itImUItp2cgiRhCgPzo8hIhDqCeaTM130_provenance.
- NP56163.RAtYRR4JS6bdqj9itImUItp2cgiRhCgPzo8hIhDqCeaTM130_assertion wasGeneratedBy ECO_0000203 NP56163.RAtYRR4JS6bdqj9itImUItp2cgiRhCgPzo8hIhDqCeaTM130_provenance.