Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[Intriguingly, mutations in ADAMTS [a disintegrin-like and metalloprotease (reprolysin-type) with thrombospondin type 1 motif] family members phenocopy these disorders, leading to recessive WMS (ADAMTS10), WMS-like syndrome (ADAMTS17), IEL (ADAMTSL4 and ADAMTS17) and GD (ADAMTSL2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP793453.RAtXK41t-w14diO4ryTqZK9Q5MHg83lmYOEOORnd3sRkY130_assertion description "[Intriguingly, mutations in ADAMTS [a disintegrin-like and metalloprotease (reprolysin-type) with thrombospondin type 1 motif] family members phenocopy these disorders, leading to recessive WMS (ADAMTS10), WMS-like syndrome (ADAMTS17), IEL (ADAMTSL4 and ADAMTS17) and GD (ADAMTSL2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP793453.RAtXK41t-w14diO4ryTqZK9Q5MHg83lmYOEOORnd3sRkY130_provenance.
• NP514503.RAYHiGF1jFgQuAh2kCXjxDObHOgWpSUbDvNPufym40Kps130_assertion description "[Intriguingly, mutations in ADAMTS [a disintegrin-like and metalloprotease (reprolysin-type) with thrombospondin type 1 motif] family members phenocopy these disorders, leading to recessive WMS (ADAMTS10), WMS-like syndrome (ADAMTS17), IEL (ADAMTSL4 and ADAMTS17) and GD (ADAMTSL2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP514503.RAYHiGF1jFgQuAh2kCXjxDObHOgWpSUbDvNPufym40Kps130_provenance.
• NP213918.RAspGf4PwFq4NAY5_RmW1v_nUiW96G67q5n4j-rf2TY6U130_assertion description "[Intriguingly, mutations in ADAMTS [a disintegrin-like and metalloprotease (reprolysin-type) with thrombospondin type 1 motif] family members phenocopy these disorders, leading to recessive WMS (ADAMTS10), WMS-like syndrome (ADAMTS17), IEL (ADAMTSL4 and ADAMTS17) and GD (ADAMTSL2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP213918.RAspGf4PwFq4NAY5_RmW1v_nUiW96G67q5n4j-rf2TY6U130_provenance.
• NP156972.RAXLMagnBB__kLVY1pjmIom8pMwfGePCVcqtXjSyS_bCU130_assertion description "[Intriguingly, mutations in ADAMTS [a disintegrin-like and metalloprotease (reprolysin-type) with thrombospondin type 1 motif] family members phenocopy these disorders, leading to recessive WMS (ADAMTS10), WMS-like syndrome (ADAMTS17), IEL (ADAMTSL4 and ADAMTS17) and GD (ADAMTSL2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP156972.RAXLMagnBB__kLVY1pjmIom8pMwfGePCVcqtXjSyS_bCU130_provenance.
• NP544590.RAuNJAY6IhJTGIu8D2veG4UBqxNOvVjZhOnGLb0bXrPYU130_assertion description "[Intriguingly, mutations in ADAMTS [a disintegrin-like and metalloprotease (reprolysin-type) with thrombospondin type 1 motif] family members phenocopy these disorders, leading to recessive WMS (ADAMTS10), WMS-like syndrome (ADAMTS17), IEL (ADAMTSL4 and ADAMTS17) and GD (ADAMTSL2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP544590.RAuNJAY6IhJTGIu8D2veG4UBqxNOvVjZhOnGLb0bXrPYU130_provenance.
• NP843554.RA7Ehl8hyv3xskbdJCuFHRjGM06r-oy2r5zt2WCT0WNXQ130_assertion description "[Intriguingly, mutations in ADAMTS [a disintegrin-like and metalloprotease (reprolysin-type) with thrombospondin type 1 motif] family members phenocopy these disorders, leading to recessive WMS (ADAMTS10), WMS-like syndrome (ADAMTS17), IEL (ADAMTSL4 and ADAMTS17) and GD (ADAMTSL2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP843554.RA7Ehl8hyv3xskbdJCuFHRjGM06r-oy2r5zt2WCT0WNXQ130_provenance.
• NP829267.RAZ5rSnri3zZ4N2RlXk3JsaCtfGj87MGRSmndUbVfCE2U130_assertion description "[Intriguingly, mutations in ADAMTS [a disintegrin-like and metalloprotease (reprolysin-type) with thrombospondin type 1 motif] family members phenocopy these disorders, leading to recessive WMS (ADAMTS10), WMS-like syndrome (ADAMTS17), IEL (ADAMTSL4 and ADAMTS17) and GD (ADAMTSL2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP829267.RAZ5rSnri3zZ4N2RlXk3JsaCtfGj87MGRSmndUbVfCE2U130_provenance.
• NP911770.RATc0guJvPghvthdrMrsVSCIi2ur1BD_o6K6sPRVrZRlQ130_assertion description "[Intriguingly, mutations in ADAMTS [a disintegrin-like and metalloprotease (reprolysin-type) with thrombospondin type 1 motif] family members phenocopy these disorders, leading to recessive WMS (ADAMTS10), WMS-like syndrome (ADAMTS17), IEL (ADAMTSL4 and ADAMTS17) and GD (ADAMTSL2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP911770.RATc0guJvPghvthdrMrsVSCIi2ur1BD_o6K6sPRVrZRlQ130_provenance.
• NP651307.RAE6-yzYnsGslvk04dns6e1gE1wJIcaIq1WK5OtbIPgxo130_assertion description "[Intriguingly, mutations in ADAMTS [a disintegrin-like and metalloprotease (reprolysin-type) with thrombospondin type 1 motif] family members phenocopy these disorders, leading to recessive WMS (ADAMTS10), WMS-like syndrome (ADAMTS17), IEL (ADAMTSL4 and ADAMTS17) and GD (ADAMTSL2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP651307.RAE6-yzYnsGslvk04dns6e1gE1wJIcaIq1WK5OtbIPgxo130_provenance.
• assertion description "[Intriguingly, mutations in ADAMTS [a disintegrin-like and metalloprotease (reprolysin-type) with thrombospondin type 1 motif] family members phenocopy these disorders, leading to recessive WMS (ADAMTS10), WMS-like syndrome (ADAMTS17), IEL (ADAMTSL4 and ADAMTS17) and GD (ADAMTSL2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Intriguingly, mutations in ADAMTS [a disintegrin-like and metalloprotease (reprolysin-type) with thrombospondin type 1 motif] family members phenocopy these disorders, leading to recessive WMS (ADAMTS10), WMS-like syndrome (ADAMTS17), IEL (ADAMTSL4 and ADAMTS17) and GD (ADAMTSL2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Intriguingly, mutations in ADAMTS [a disintegrin-like and metalloprotease (reprolysin-type) with thrombospondin type 1 motif] family members phenocopy these disorders, leading to recessive WMS (ADAMTS10), WMS-like syndrome (ADAMTS17), IEL (ADAMTSL4 and ADAMTS17) and GD (ADAMTSL2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Intriguingly, mutations in ADAMTS [a disintegrin-like and metalloprotease (reprolysin-type) with thrombospondin type 1 motif] family members phenocopy these disorders, leading to recessive WMS (ADAMTS10), WMS-like syndrome (ADAMTS17), IEL (ADAMTSL4 and ADAMTS17) and GD (ADAMTSL2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Intriguingly, mutations in ADAMTS [a disintegrin-like and metalloprotease (reprolysin-type) with thrombospondin type 1 motif] family members phenocopy these disorders, leading to recessive WMS (ADAMTS10), WMS-like syndrome (ADAMTS17), IEL (ADAMTSL4 and ADAMTS17) and GD (ADAMTSL2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Intriguingly, mutations in ADAMTS [a disintegrin-like and metalloprotease (reprolysin-type) with thrombospondin type 1 motif] family members phenocopy these disorders, leading to recessive WMS (ADAMTS10), WMS-like syndrome (ADAMTS17), IEL (ADAMTSL4 and ADAMTS17) and GD (ADAMTSL2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Intriguingly, mutations in ADAMTS [a disintegrin-like and metalloprotease (reprolysin-type) with thrombospondin type 1 motif] family members phenocopy these disorders, leading to recessive WMS (ADAMTS10), WMS-like syndrome (ADAMTS17), IEL (ADAMTSL4 and ADAMTS17) and GD (ADAMTSL2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP918454.RAc8vhxsAjHyV3ujeDl37ktrXoUjECGqE_uDG07aBprSc130_assertion description "[Intriguingly, mutations in ADAMTS [a disintegrin-like and metalloprotease (reprolysin-type) with thrombospondin type 1 motif] family members phenocopy these disorders, leading to recessive WMS (ADAMTS10), WMS-like syndrome (ADAMTS17), IEL (ADAMTSL4 and ADAMTS17) and GD (ADAMTSL2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP918454.RAc8vhxsAjHyV3ujeDl37ktrXoUjECGqE_uDG07aBprSc130_provenance.
• NP799300.RAM-x6_2k98RakIsdO6bQvLqVu-A8j3dXghuz2mwDsQrI130_assertion description "[Intriguingly, mutations in ADAMTS [a disintegrin-like and metalloprotease (reprolysin-type) with thrombospondin type 1 motif] family members phenocopy these disorders, leading to recessive WMS (ADAMTS10), WMS-like syndrome (ADAMTS17), IEL (ADAMTSL4 and ADAMTS17) and GD (ADAMTSL2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP799300.RAM-x6_2k98RakIsdO6bQvLqVu-A8j3dXghuz2mwDsQrI130_provenance.
• NP911782.RApeVGLC3qyB2X-rB2GdUOVwJBzs-Tl0J1UtXlEvWOvuw130_assertion description "[Intriguingly, mutations in ADAMTS [a disintegrin-like and metalloprotease (reprolysin-type) with thrombospondin type 1 motif] family members phenocopy these disorders, leading to recessive WMS (ADAMTS10), WMS-like syndrome (ADAMTS17), IEL (ADAMTSL4 and ADAMTS17) and GD (ADAMTSL2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP911782.RApeVGLC3qyB2X-rB2GdUOVwJBzs-Tl0J1UtXlEvWOvuw130_provenance.
• NP914275.RAOxDfJQGillxEVqcF-TVtqqb2iS0HzKMqueE4wt1rbbk130_assertion description "[Intriguingly, mutations in ADAMTS [a disintegrin-like and metalloprotease (reprolysin-type) with thrombospondin type 1 motif] family members phenocopy these disorders, leading to recessive WMS (ADAMTS10), WMS-like syndrome (ADAMTS17), IEL (ADAMTSL4 and ADAMTS17) and GD (ADAMTSL2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP914275.RAOxDfJQGillxEVqcF-TVtqqb2iS0HzKMqueE4wt1rbbk130_provenance.
• NP918455.RAtO5wWIhov9SjC9nPvZliX9oSEPrv8vK064a_F-EFrbs130_assertion description "[Intriguingly, mutations in ADAMTS [a disintegrin-like and metalloprotease (reprolysin-type) with thrombospondin type 1 motif] family members phenocopy these disorders, leading to recessive WMS (ADAMTS10), WMS-like syndrome (ADAMTS17), IEL (ADAMTSL4 and ADAMTS17) and GD (ADAMTSL2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP918455.RAtO5wWIhov9SjC9nPvZliX9oSEPrv8vK064a_F-EFrbs130_provenance.
• NP918457.RAkQohCJXZIl92yzJFhnE5TAIJto2tW8d2oWAmssDyfEM130_assertion description "[Intriguingly, mutations in ADAMTS [a disintegrin-like and metalloprotease (reprolysin-type) with thrombospondin type 1 motif] family members phenocopy these disorders, leading to recessive WMS (ADAMTS10), WMS-like syndrome (ADAMTS17), IEL (ADAMTSL4 and ADAMTS17) and GD (ADAMTSL2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP918457.RAkQohCJXZIl92yzJFhnE5TAIJto2tW8d2oWAmssDyfEM130_provenance.
• NP918451.RAJSbr9xU1OzLhsclJhKNB_1FvmwRK_oH8n3f6aMV1rEU130_assertion description "[Intriguingly, mutations in ADAMTS [a disintegrin-like and metalloprotease (reprolysin-type) with thrombospondin type 1 motif] family members phenocopy these disorders, leading to recessive WMS (ADAMTS10), WMS-like syndrome (ADAMTS17), IEL (ADAMTSL4 and ADAMTS17) and GD (ADAMTSL2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP918451.RAJSbr9xU1OzLhsclJhKNB_1FvmwRK_oH8n3f6aMV1rEU130_provenance.
• NP829272.RAwZDHXJzfWxIkACYtCif9cV_5VLMgYFPeBg4FMXrNJj8130_assertion description "[Intriguingly, mutations in ADAMTS [a disintegrin-like and metalloprotease (reprolysin-type) with thrombospondin type 1 motif] family members phenocopy these disorders, leading to recessive WMS (ADAMTS10), WMS-like syndrome (ADAMTS17), IEL (ADAMTSL4 and ADAMTS17) and GD (ADAMTSL2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP829272.RAwZDHXJzfWxIkACYtCif9cV_5VLMgYFPeBg4FMXrNJj8130_provenance.
• NP911777.RAwYxN77NCMohTGXZP8U14eyohZ7CMnrCGBfDGCBEnXog130_assertion description "[Intriguingly, mutations in ADAMTS [a disintegrin-like and metalloprotease (reprolysin-type) with thrombospondin type 1 motif] family members phenocopy these disorders, leading to recessive WMS (ADAMTS10), WMS-like syndrome (ADAMTS17), IEL (ADAMTSL4 and ADAMTS17) and GD (ADAMTSL2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP911777.RAwYxN77NCMohTGXZP8U14eyohZ7CMnrCGBfDGCBEnXog130_provenance.
• NP918456.RA9a9Kj_t7TXwgHzbJNWNKrqmVpxy-kV_ejD5U564GGVw130_assertion description "[Intriguingly, mutations in ADAMTS [a disintegrin-like and metalloprotease (reprolysin-type) with thrombospondin type 1 motif] family members phenocopy these disorders, leading to recessive WMS (ADAMTS10), WMS-like syndrome (ADAMTS17), IEL (ADAMTSL4 and ADAMTS17) and GD (ADAMTSL2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP918456.RA9a9Kj_t7TXwgHzbJNWNKrqmVpxy-kV_ejD5U564GGVw130_provenance.