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- NP263358.RAtc9h6A97nJsFeSf3NkwxmD40cBIJgS2_8xlkoDQCeOc130_assertion type Assertion NP263358.RAtc9h6A97nJsFeSf3NkwxmD40cBIJgS2_8xlkoDQCeOc130_head.
- NP263358.RAtc9h6A97nJsFeSf3NkwxmD40cBIJgS2_8xlkoDQCeOc130_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." NP263358.RAtc9h6A97nJsFeSf3NkwxmD40cBIJgS2_8xlkoDQCeOc130_provenance.
- NP263358.RAtc9h6A97nJsFeSf3NkwxmD40cBIJgS2_8xlkoDQCeOc130_assertion evidence source_evidence_literature NP263358.RAtc9h6A97nJsFeSf3NkwxmD40cBIJgS2_8xlkoDQCeOc130_provenance.
- NP263358.RAtc9h6A97nJsFeSf3NkwxmD40cBIJgS2_8xlkoDQCeOc130_assertion SIO_000772 21106043 NP263358.RAtc9h6A97nJsFeSf3NkwxmD40cBIJgS2_8xlkoDQCeOc130_provenance.
- NP263358.RAtc9h6A97nJsFeSf3NkwxmD40cBIJgS2_8xlkoDQCeOc130_assertion wasDerivedFrom befree-20140225 NP263358.RAtc9h6A97nJsFeSf3NkwxmD40cBIJgS2_8xlkoDQCeOc130_provenance.
- NP263358.RAtc9h6A97nJsFeSf3NkwxmD40cBIJgS2_8xlkoDQCeOc130_assertion wasGeneratedBy ECO_0000203 NP263358.RAtc9h6A97nJsFeSf3NkwxmD40cBIJgS2_8xlkoDQCeOc130_provenance.