Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[KTS (lysine-threonine-serine) splice site mutations in WT1 intron 9 have been described in patients with Frasier syndrome, another rare syndrome defined by focal and segmental glomerulosclerosis (FSGS), XY pseudohermaphroditism, and frequent occurrence of gonadoblastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP545718.RAaxiH0rwRYF6q6ESQqwliez6GCVvTbGAVE9TMJCkoMUk130_assertion description "[KTS (lysine-threonine-serine) splice site mutations in WT1 intron 9 have been described in patients with Frasier syndrome, another rare syndrome defined by focal and segmental glomerulosclerosis (FSGS), XY pseudohermaphroditism, and frequent occurrence of gonadoblastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP545718.RAaxiH0rwRYF6q6ESQqwliez6GCVvTbGAVE9TMJCkoMUk130_provenance.
• NP433914.RAkB1mPbZDqSCHGD6zohcEF6KPKseN9hM0BWOEKcip3vo130_assertion description "[KTS (lysine-threonine-serine) splice site mutations in WT1 intron 9 have been described in patients with Frasier syndrome, another rare syndrome defined by focal and segmental glomerulosclerosis (FSGS), XY pseudohermaphroditism, and frequent occurrence of gonadoblastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP433914.RAkB1mPbZDqSCHGD6zohcEF6KPKseN9hM0BWOEKcip3vo130_provenance.
• NP716165.RArB9ZYUtwyiiw7RE0kTBK_nfs91WAucEdWc_5DX_y_Nw130_assertion description "[KTS (lysine-threonine-serine) splice site mutations in WT1 intron 9 have been described in patients with Frasier syndrome, another rare syndrome defined by focal and segmental glomerulosclerosis (FSGS), XY pseudohermaphroditism, and frequent occurrence of gonadoblastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP716165.RArB9ZYUtwyiiw7RE0kTBK_nfs91WAucEdWc_5DX_y_Nw130_provenance.
• NP554002.RAjceSEUlI4q5Ggt88Qat15pCHI6ynH7yTI3Lx7iGAcGI130_assertion description "[KTS (lysine-threonine-serine) splice site mutations in WT1 intron 9 have been described in patients with Frasier syndrome, another rare syndrome defined by focal and segmental glomerulosclerosis (FSGS), XY pseudohermaphroditism, and frequent occurrence of gonadoblastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP554002.RAjceSEUlI4q5Ggt88Qat15pCHI6ynH7yTI3Lx7iGAcGI130_provenance.
• NP346410.RAMQwCSNgA8XSQhReg1WVKF-sxAJblyu4iref8rWVCYOk130_assertion description "[KTS (lysine-threonine-serine) splice site mutations in WT1 intron 9 have been described in patients with Frasier syndrome, another rare syndrome defined by focal and segmental glomerulosclerosis (FSGS), XY pseudohermaphroditism, and frequent occurrence of gonadoblastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP346410.RAMQwCSNgA8XSQhReg1WVKF-sxAJblyu4iref8rWVCYOk130_provenance.
• NP750538.RA33-v9IozeJCjkRP5sM6EtBkEFRvPYq8UFS4Xas8sp6w130_assertion description "[KTS (lysine-threonine-serine) splice site mutations in WT1 intron 9 have been described in patients with Frasier syndrome, another rare syndrome defined by focal and segmental glomerulosclerosis (FSGS), XY pseudohermaphroditism, and frequent occurrence of gonadoblastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP750538.RA33-v9IozeJCjkRP5sM6EtBkEFRvPYq8UFS4Xas8sp6w130_provenance.
• NP539182.RAPfSKp0WbQc81djQVAqk97xPled4scPEmy7mTCHFfzSk130_assertion description "[KTS (lysine-threonine-serine) splice site mutations in WT1 intron 9 have been described in patients with Frasier syndrome, another rare syndrome defined by focal and segmental glomerulosclerosis (FSGS), XY pseudohermaphroditism, and frequent occurrence of gonadoblastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP539182.RAPfSKp0WbQc81djQVAqk97xPled4scPEmy7mTCHFfzSk130_provenance.
• NP1011446.RASi_0nZjhSUTC1W7WQzuV4YVjeArMIu267EyVP9NyK3g130_assertion description "[KTS (lysine-threonine-serine) splice site mutations in WT1 intron 9 have been described in patients with Frasier syndrome, another rare syndrome defined by focal and segmental glomerulosclerosis (FSGS), XY pseudohermaphroditism, and frequent occurrence of gonadoblastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1011446.RASi_0nZjhSUTC1W7WQzuV4YVjeArMIu267EyVP9NyK3g130_provenance.
• NP264485.RAUlJ3ZYMdtQuyEFD2RGW0pjiT6yLPKAXJ81umzUIbOto130_assertion description "[KTS (lysine-threonine-serine) splice site mutations in WT1 intron 9 have been described in patients with Frasier syndrome, another rare syndrome defined by focal and segmental glomerulosclerosis (FSGS), XY pseudohermaphroditism, and frequent occurrence of gonadoblastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP264485.RAUlJ3ZYMdtQuyEFD2RGW0pjiT6yLPKAXJ81umzUIbOto130_provenance.
• assertion description "[KTS (lysine-threonine-serine) splice site mutations in WT1 intron 9 have been described in patients with Frasier syndrome, another rare syndrome defined by focal and segmental glomerulosclerosis (FSGS), XY pseudohermaphroditism, and frequent occurrence of gonadoblastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.