Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP218904.RAY7dLJ10Rq3Any_mx3812Vq1bD76YbcccqfKVpRFcrRw130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP218904.RAY7dLJ10Rq3Any_mx3812Vq1bD76YbcccqfKVpRFcrRw130_assertion type Assertion NP218904.RAY7dLJ10Rq3Any_mx3812Vq1bD76YbcccqfKVpRFcrRw130_head.
- NP218904.RAY7dLJ10Rq3Any_mx3812Vq1bD76YbcccqfKVpRFcrRw130_assertion description "[A variant located at the 3' UTR of the FGF2 gene (rs6820411) was highly associated with atrophic AMD, and the functional SNP rs3112831 at ABCA4 showed a marginal association with the disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP218904.RAY7dLJ10Rq3Any_mx3812Vq1bD76YbcccqfKVpRFcrRw130_provenance.
- NP218904.RAY7dLJ10Rq3Any_mx3812Vq1bD76YbcccqfKVpRFcrRw130_assertion evidence source_evidence_literature NP218904.RAY7dLJ10Rq3Any_mx3812Vq1bD76YbcccqfKVpRFcrRw130_provenance.
- NP218904.RAY7dLJ10Rq3Any_mx3812Vq1bD76YbcccqfKVpRFcrRw130_assertion SIO_000772 21106043 NP218904.RAY7dLJ10Rq3Any_mx3812Vq1bD76YbcccqfKVpRFcrRw130_provenance.
- NP218904.RAY7dLJ10Rq3Any_mx3812Vq1bD76YbcccqfKVpRFcrRw130_assertion wasDerivedFrom befree-20150227 NP218904.RAY7dLJ10Rq3Any_mx3812Vq1bD76YbcccqfKVpRFcrRw130_provenance.
- NP218904.RAY7dLJ10Rq3Any_mx3812Vq1bD76YbcccqfKVpRFcrRw130_assertion wasGeneratedBy ECO_0000203 NP218904.RAY7dLJ10Rq3Any_mx3812Vq1bD76YbcccqfKVpRFcrRw130_provenance.