Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[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."@en ?g. }

• NP855964.RAAoRxIAYCTM31lKfug5qPHlATlBlW-kVN6aYE08sZfOs130_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." NP855964.RAAoRxIAYCTM31lKfug5qPHlATlBlW-kVN6aYE08sZfOs130_provenance.
• NP902295.RAAt1_rPhrTfCME7ft9j-oB2pVc1kZnTD7i65EDcZtVfc130_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." NP902295.RAAt1_rPhrTfCME7ft9j-oB2pVc1kZnTD7i65EDcZtVfc130_provenance.
• NP615364.RAT5TrFP6RyADL_gdouA5CWqvwknwNRnA9JXOx0IAVXsY130_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." NP615364.RAT5TrFP6RyADL_gdouA5CWqvwknwNRnA9JXOx0IAVXsY130_provenance.
• 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." provenance.
• NP219742.RAs9XE9Qc_zyN7oIIaBB-gfWCNvcd9minJA4QbroARdMs130_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." NP219742.RAs9XE9Qc_zyN7oIIaBB-gfWCNvcd9minJA4QbroARdMs130_provenance.
• 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.
• 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." provenance.
• 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." provenance.
• NP180341.RAFuW7bDG1tgXlVLkLV1gqTCtnM19Ys9RLWlGdgAmraSQ130_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." NP180341.RAFuW7bDG1tgXlVLkLV1gqTCtnM19Ys9RLWlGdgAmraSQ130_provenance.
• NP563004.RA1bP0Yjc9AvInm65F0rBO0C6li77sBNu2_J3T6JNvJAY130_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." NP563004.RA1bP0Yjc9AvInm65F0rBO0C6li77sBNu2_J3T6JNvJAY130_provenance.
• NP805596.RA8uGaOe4OFYzKLJtYi6inZ9EJTtvm3IBD-adIgLI2bN8130_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." NP805596.RA8uGaOe4OFYzKLJtYi6inZ9EJTtvm3IBD-adIgLI2bN8130_provenance.
• 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.
• NP399998.RAcfCuNmQHZ3V4WOdJAdOZot9I-E1rMbQp9VFgIhIRj60130_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." NP399998.RAcfCuNmQHZ3V4WOdJAdOZot9I-E1rMbQp9VFgIhIRj60130_provenance.
• NP432248.RAWIQ9o2LfArakLCVJNJEa6QwsusDhR0cKaiV2oE4hElw130_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." NP432248.RAWIQ9o2LfArakLCVJNJEa6QwsusDhR0cKaiV2oE4hElw130_provenance.
• NP758278.RAPPO4jJrPdqxyolZ4uuCcVy0GtGCESiRjVqf-5W92rhM130_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." NP758278.RAPPO4jJrPdqxyolZ4uuCcVy0GtGCESiRjVqf-5W92rhM130_provenance.
• NP432294.RADzBjnXqt888h4ngHnIWHk1Dmc6hnjYPSslojba4WP-E130_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." NP432294.RADzBjnXqt888h4ngHnIWHk1Dmc6hnjYPSslojba4WP-E130_provenance.
• NP854530.RAgg1Vnq5c9KmXVgrlQh7pY0zKWy3YU7dNygfStS3bL1E130_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." NP854530.RAgg1Vnq5c9KmXVgrlQh7pY0zKWy3YU7dNygfStS3bL1E130_provenance.
• NP854543.RAh2exYm1Q_mmvOjlguLs_3Ma0ajUl8xoHisDjcKkg1Co130_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." NP854543.RAh2exYm1Q_mmvOjlguLs_3Ma0ajUl8xoHisDjcKkg1Co130_provenance.
• NP400012.RA-zCLEccWFyKL9hZVV6CwtqBt1SQU5OYZldM2I1N6i3A130_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." NP400012.RA-zCLEccWFyKL9hZVV6CwtqBt1SQU5OYZldM2I1N6i3A130_provenance.
• NP854540.RAzp5wmxrW5IZI-eXSzvCr70aRPSAABpTH3EJsU8zBj3g130_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." NP854540.RAzp5wmxrW5IZI-eXSzvCr70aRPSAABpTH3EJsU8zBj3g130_provenance.