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Matches in Nanopublications for { ?s ?p "[We identified chromosomal deletions within the WASP gene in two patients with Wiskott-Aldrich syndrome; a missense mutation in a patient with X-linked thrombocytopenia; and mutations in the RUNX1 gene of five patients with familial platelet disorder with propensity to acute myelogenous leukemia, and in the ANKRD26 gene of four patients with autosomal dominant thrombocytopenia-2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• assertion description "[We identified chromosomal deletions within the WASP gene in two patients with Wiskott-Aldrich syndrome; a missense mutation in a patient with X-linked thrombocytopenia; and mutations in the RUNX1 gene of five patients with familial platelet disorder with propensity to acute myelogenous leukemia, and in the ANKRD26 gene of four patients with autosomal dominant thrombocytopenia-2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[We identified chromosomal deletions within the WASP gene in two patients with Wiskott-Aldrich syndrome; a missense mutation in a patient with X-linked thrombocytopenia; and mutations in the RUNX1 gene of five patients with familial platelet disorder with propensity to acute myelogenous leukemia, and in the ANKRD26 gene of four patients with autosomal dominant thrombocytopenia-2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[We identified chromosomal deletions within the WASP gene in two patients with Wiskott-Aldrich syndrome; a missense mutation in a patient with X-linked thrombocytopenia; and mutations in the RUNX1 gene of five patients with familial platelet disorder with propensity to acute myelogenous leukemia, and in the ANKRD26 gene of four patients with autosomal dominant thrombocytopenia-2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[We identified chromosomal deletions within the WASP gene in two patients with Wiskott-Aldrich syndrome; a missense mutation in a patient with X-linked thrombocytopenia; and mutations in the RUNX1 gene of five patients with familial platelet disorder with propensity to acute myelogenous leukemia, and in the ANKRD26 gene of four patients with autosomal dominant thrombocytopenia-2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[We identified chromosomal deletions within the WASP gene in two patients with Wiskott-Aldrich syndrome; a missense mutation in a patient with X-linked thrombocytopenia; and mutations in the RUNX1 gene of five patients with familial platelet disorder with propensity to acute myelogenous leukemia, and in the ANKRD26 gene of four patients with autosomal dominant thrombocytopenia-2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[We identified chromosomal deletions within the WASP gene in two patients with Wiskott-Aldrich syndrome; a missense mutation in a patient with X-linked thrombocytopenia; and mutations in the RUNX1 gene of five patients with familial platelet disorder with propensity to acute myelogenous leukemia, and in the ANKRD26 gene of four patients with autosomal dominant thrombocytopenia-2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP1290136.RAeIzCFJKAjMwR0IGFYCORtjYcLlpIMyV2F6qHamq64KE130_assertion description "[We identified chromosomal deletions within the WASP gene in two patients with Wiskott-Aldrich syndrome; a missense mutation in a patient with X-linked thrombocytopenia; and mutations in the RUNX1 gene of five patients with familial platelet disorder with propensity to acute myelogenous leukemia, and in the ANKRD26 gene of four patients with autosomal dominant thrombocytopenia-2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1290136.RAeIzCFJKAjMwR0IGFYCORtjYcLlpIMyV2F6qHamq64KE130_provenance.
• NP1290139.RAbcgW29khDjqdfqaApX3GPRiVBXFmce486QIqSR0l-90130_assertion description "[We identified chromosomal deletions within the WASP gene in two patients with Wiskott-Aldrich syndrome; a missense mutation in a patient with X-linked thrombocytopenia; and mutations in the RUNX1 gene of five patients with familial platelet disorder with propensity to acute myelogenous leukemia, and in the ANKRD26 gene of four patients with autosomal dominant thrombocytopenia-2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1290139.RAbcgW29khDjqdfqaApX3GPRiVBXFmce486QIqSR0l-90130_provenance.
• NP1290141.RAYvh_2SwnmJ_dZ8_p1okNzy1_OH-kP9Ut29vYx9rPteI130_assertion description "[We identified chromosomal deletions within the WASP gene in two patients with Wiskott-Aldrich syndrome; a missense mutation in a patient with X-linked thrombocytopenia; and mutations in the RUNX1 gene of five patients with familial platelet disorder with propensity to acute myelogenous leukemia, and in the ANKRD26 gene of four patients with autosomal dominant thrombocytopenia-2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1290141.RAYvh_2SwnmJ_dZ8_p1okNzy1_OH-kP9Ut29vYx9rPteI130_provenance.
• NP1290132.RAoq12IjBAuYTovgIjmRHeVtrXVyMrp5uARuhetQ1etHo130_assertion description "[We identified chromosomal deletions within the WASP gene in two patients with Wiskott-Aldrich syndrome; a missense mutation in a patient with X-linked thrombocytopenia; and mutations in the RUNX1 gene of five patients with familial platelet disorder with propensity to acute myelogenous leukemia, and in the ANKRD26 gene of four patients with autosomal dominant thrombocytopenia-2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1290132.RAoq12IjBAuYTovgIjmRHeVtrXVyMrp5uARuhetQ1etHo130_provenance.
• NP1290138.RAvAU8ozh7G1qbpOb_4s9AKkWsMyYNdXkAQk1xJ0V-Jb4130_assertion description "[We identified chromosomal deletions within the WASP gene in two patients with Wiskott-Aldrich syndrome; a missense mutation in a patient with X-linked thrombocytopenia; and mutations in the RUNX1 gene of five patients with familial platelet disorder with propensity to acute myelogenous leukemia, and in the ANKRD26 gene of four patients with autosomal dominant thrombocytopenia-2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1290138.RAvAU8ozh7G1qbpOb_4s9AKkWsMyYNdXkAQk1xJ0V-Jb4130_provenance.
• NP1290140.RAhs5bsYLfrJd8MYD-WX56Mn30gHLMRhWdoIOYCEbSdqk130_assertion description "[We identified chromosomal deletions within the WASP gene in two patients with Wiskott-Aldrich syndrome; a missense mutation in a patient with X-linked thrombocytopenia; and mutations in the RUNX1 gene of five patients with familial platelet disorder with propensity to acute myelogenous leukemia, and in the ANKRD26 gene of four patients with autosomal dominant thrombocytopenia-2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1290140.RAhs5bsYLfrJd8MYD-WX56Mn30gHLMRhWdoIOYCEbSdqk130_provenance.
• NP1290142.RAopO0axpxFy8HkinWkO4tVYhtHOBgaEGYtmNNLb-Y2OY130_assertion description "[We identified chromosomal deletions within the WASP gene in two patients with Wiskott-Aldrich syndrome; a missense mutation in a patient with X-linked thrombocytopenia; and mutations in the RUNX1 gene of five patients with familial platelet disorder with propensity to acute myelogenous leukemia, and in the ANKRD26 gene of four patients with autosomal dominant thrombocytopenia-2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1290142.RAopO0axpxFy8HkinWkO4tVYhtHOBgaEGYtmNNLb-Y2OY130_provenance.
• NP1290131.RANV3e7te99SWYHVi1RZScdLfdJVRnZEn3av4GshfGrBw130_assertion description "[We identified chromosomal deletions within the WASP gene in two patients with Wiskott-Aldrich syndrome; a missense mutation in a patient with X-linked thrombocytopenia; and mutations in the RUNX1 gene of five patients with familial platelet disorder with propensity to acute myelogenous leukemia, and in the ANKRD26 gene of four patients with autosomal dominant thrombocytopenia-2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1290131.RANV3e7te99SWYHVi1RZScdLfdJVRnZEn3av4GshfGrBw130_provenance.
• NP1290135.RAHDuhtm9iQUUVLk-Jehtj-LFqre7gR2ls-WpJgBL0Rr8130_assertion description "[We identified chromosomal deletions within the WASP gene in two patients with Wiskott-Aldrich syndrome; a missense mutation in a patient with X-linked thrombocytopenia; and mutations in the RUNX1 gene of five patients with familial platelet disorder with propensity to acute myelogenous leukemia, and in the ANKRD26 gene of four patients with autosomal dominant thrombocytopenia-2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1290135.RAHDuhtm9iQUUVLk-Jehtj-LFqre7gR2ls-WpJgBL0Rr8130_provenance.
• NP1290137.RAOjRvXR7TbxYTh5EPYZqtdMRBVaSNPQhkelLw_Pqsgmg130_assertion description "[We identified chromosomal deletions within the WASP gene in two patients with Wiskott-Aldrich syndrome; a missense mutation in a patient with X-linked thrombocytopenia; and mutations in the RUNX1 gene of five patients with familial platelet disorder with propensity to acute myelogenous leukemia, and in the ANKRD26 gene of four patients with autosomal dominant thrombocytopenia-2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1290137.RAOjRvXR7TbxYTh5EPYZqtdMRBVaSNPQhkelLw_Pqsgmg130_provenance.
• NP1290133.RAwYfB_5ivdNGtPfpU_kB1peHZQNRyYv96kMyo7rWYXR8130_assertion description "[We identified chromosomal deletions within the WASP gene in two patients with Wiskott-Aldrich syndrome; a missense mutation in a patient with X-linked thrombocytopenia; and mutations in the RUNX1 gene of five patients with familial platelet disorder with propensity to acute myelogenous leukemia, and in the ANKRD26 gene of four patients with autosomal dominant thrombocytopenia-2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1290133.RAwYfB_5ivdNGtPfpU_kB1peHZQNRyYv96kMyo7rWYXR8130_provenance.
• NP1290134.RA9g1HF8BXsL8yBlcolHGbov55c7jLqjPH0Sw1V7-EZz8130_assertion description "[We identified chromosomal deletions within the WASP gene in two patients with Wiskott-Aldrich syndrome; a missense mutation in a patient with X-linked thrombocytopenia; and mutations in the RUNX1 gene of five patients with familial platelet disorder with propensity to acute myelogenous leukemia, and in the ANKRD26 gene of four patients with autosomal dominant thrombocytopenia-2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1290134.RA9g1HF8BXsL8yBlcolHGbov55c7jLqjPH0Sw1V7-EZz8130_provenance.