Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[Three patients had a Gly1961Glu missense mutation, the most common variant in Stargardt disease (STGD), with 2 of these subjects having a macular dystrophy (MD) phenotype and a second ABCA4 variant previously associated with STGD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• assertion description "[Three patients had a Gly1961Glu missense mutation, the most common variant in Stargardt disease (STGD), with 2 of these subjects having a macular dystrophy (MD) phenotype and a second ABCA4 variant previously associated with STGD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Three patients had a Gly1961Glu missense mutation, the most common variant in Stargardt disease (STGD), with 2 of these subjects having a macular dystrophy (MD) phenotype and a second ABCA4 variant previously associated with STGD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Three patients had a Gly1961Glu missense mutation, the most common variant in Stargardt disease (STGD), with 2 of these subjects having a macular dystrophy (MD) phenotype and a second ABCA4 variant previously associated with STGD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Three patients had a Gly1961Glu missense mutation, the most common variant in Stargardt disease (STGD), with 2 of these subjects having a macular dystrophy (MD) phenotype and a second ABCA4 variant previously associated with STGD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP315413.RAMG7qHOi4gjDZQe_6TwS2-SQax7UJuP8UiUMmPZBzjAE130_assertion description "[Three patients had a Gly1961Glu missense mutation, the most common variant in Stargardt disease (STGD), with 2 of these subjects having a macular dystrophy (MD) phenotype and a second ABCA4 variant previously associated with STGD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP315413.RAMG7qHOi4gjDZQe_6TwS2-SQax7UJuP8UiUMmPZBzjAE130_provenance.
• NP706105.RAEysI9AnkAJ9ZQP8SKYLRbgWAVf3jC57vAhCGHJRNnI8130_assertion description "[Three patients had a Gly1961Glu missense mutation, the most common variant in Stargardt disease (STGD), with 2 of these subjects having a macular dystrophy (MD) phenotype and a second ABCA4 variant previously associated with STGD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP706105.RAEysI9AnkAJ9ZQP8SKYLRbgWAVf3jC57vAhCGHJRNnI8130_provenance.
• NP641151.RAc64SHeJ-bOQHsS8-Hxjpv0gdVDNzyfquwQ1xTdQHTxU130_assertion description "[Three patients had a Gly1961Glu missense mutation, the most common variant in Stargardt disease (STGD), with 2 of these subjects having a macular dystrophy (MD) phenotype and a second ABCA4 variant previously associated with STGD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP641151.RAc64SHeJ-bOQHsS8-Hxjpv0gdVDNzyfquwQ1xTdQHTxU130_provenance.
• NP218936.RAkkeaN7un4JnAUHby2Rt-bxGU7xsv1MVT0ZnJK1U8H9Y130_assertion description "[Three patients had a Gly1961Glu missense mutation, the most common variant in Stargardt disease (STGD), with 2 of these subjects having a macular dystrophy (MD) phenotype and a second ABCA4 variant previously associated with STGD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP218936.RAkkeaN7un4JnAUHby2Rt-bxGU7xsv1MVT0ZnJK1U8H9Y130_provenance.
• NP218969.RABos-OruXk72o_zbRyO0usWgij6cnazhgn1T5bSdJXwk130_assertion description "[Three patients had a Gly1961Glu missense mutation, the most common variant in Stargardt disease (STGD), with 2 of these subjects having a macular dystrophy (MD) phenotype and a second ABCA4 variant previously associated with STGD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP218969.RABos-OruXk72o_zbRyO0usWgij6cnazhgn1T5bSdJXwk130_provenance.
• NP641154.RAnfHlind5spGKlXmV-3e52kbr-0Vk5Ow6_B0vOzFrAnU130_assertion description "[Three patients had a Gly1961Glu missense mutation, the most common variant in Stargardt disease (STGD), with 2 of these subjects having a macular dystrophy (MD) phenotype and a second ABCA4 variant previously associated with STGD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP641154.RAnfHlind5spGKlXmV-3e52kbr-0Vk5Ow6_B0vOzFrAnU130_provenance.
• NP218853.RAwekyqlf2LQZV5wNHzEsvK78zXdCVDOCn-t525ar3VYE130_assertion description "[Three patients had a Gly1961Glu missense mutation, the most common variant in Stargardt disease (STGD), with 2 of these subjects having a macular dystrophy (MD) phenotype and a second ABCA4 variant previously associated with STGD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP218853.RAwekyqlf2LQZV5wNHzEsvK78zXdCVDOCn-t525ar3VYE130_provenance.
• NP641152.RAJMMiQqSkUyr8N0mRtjxVo5QUuqZdqaemciAg6G2BUkk130_assertion description "[Three patients had a Gly1961Glu missense mutation, the most common variant in Stargardt disease (STGD), with 2 of these subjects having a macular dystrophy (MD) phenotype and a second ABCA4 variant previously associated with STGD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP641152.RAJMMiQqSkUyr8N0mRtjxVo5QUuqZdqaemciAg6G2BUkk130_provenance.
• NP641153.RAOyaeH29pmhqiJaQG9aimNOfOC90xX3GyQsITKMiZf2c130_assertion description "[Three patients had a Gly1961Glu missense mutation, the most common variant in Stargardt disease (STGD), with 2 of these subjects having a macular dystrophy (MD) phenotype and a second ABCA4 variant previously associated with STGD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP641153.RAOyaeH29pmhqiJaQG9aimNOfOC90xX3GyQsITKMiZf2c130_provenance.