Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[Mutations in the SP110 gene result in infantile onset of the autosomal recessive primary immunodeficiency disease veno-occlusive disease with immunodeficiency syndrome (VODI), which is characterized by hypogammaglobulinemia, T-cell dysfunction, and a high frequency of hepatic veno-occlusive disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP737303.RACyvapXZ_CdsEQBilNb9dRZAw9FH6SrBZPL_f8ojNNAU130_assertion description "[Mutations in the SP110 gene result in infantile onset of the autosomal recessive primary immunodeficiency disease veno-occlusive disease with immunodeficiency syndrome (VODI), which is characterized by hypogammaglobulinemia, T-cell dysfunction, and a high frequency of hepatic veno-occlusive disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP737303.RACyvapXZ_CdsEQBilNb9dRZAw9FH6SrBZPL_f8ojNNAU130_provenance.
• NP223709.RAA-P1VET0GA8R90izbVu53z_CCrXyViWQJycvn3v6htc130_assertion description "[Mutations in the SP110 gene result in infantile onset of the autosomal recessive primary immunodeficiency disease veno-occlusive disease with immunodeficiency syndrome (VODI), which is characterized by hypogammaglobulinemia, T-cell dysfunction, and a high frequency of hepatic veno-occlusive disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP223709.RAA-P1VET0GA8R90izbVu53z_CCrXyViWQJycvn3v6htc130_provenance.
• NP282981.RAs6Zw7j_BGWumxGTJLcpNKYeOBwbTnvUVae-y8aQtdSc130_assertion description "[Mutations in the SP110 gene result in infantile onset of the autosomal recessive primary immunodeficiency disease veno-occlusive disease with immunodeficiency syndrome (VODI), which is characterized by hypogammaglobulinemia, T-cell dysfunction, and a high frequency of hepatic veno-occlusive disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP282981.RAs6Zw7j_BGWumxGTJLcpNKYeOBwbTnvUVae-y8aQtdSc130_provenance.
• NP661488.RAhkoV39L4MKAiVoZmDiPW9ofhbbSYiESF7rQnAIo64DQ130_assertion description "[Mutations in the SP110 gene result in infantile onset of the autosomal recessive primary immunodeficiency disease veno-occlusive disease with immunodeficiency syndrome (VODI), which is characterized by hypogammaglobulinemia, T-cell dysfunction, and a high frequency of hepatic veno-occlusive disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP661488.RAhkoV39L4MKAiVoZmDiPW9ofhbbSYiESF7rQnAIo64DQ130_provenance.
• NP837246.RArcNDMeM3Q1hc9J7ffcHffIPlSYdwsQvHNx6VwmsmnMQ130_assertion description "[Mutations in the SP110 gene result in infantile onset of the autosomal recessive primary immunodeficiency disease veno-occlusive disease with immunodeficiency syndrome (VODI), which is characterized by hypogammaglobulinemia, T-cell dysfunction, and a high frequency of hepatic veno-occlusive disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP837246.RArcNDMeM3Q1hc9J7ffcHffIPlSYdwsQvHNx6VwmsmnMQ130_provenance.
• NP632347.RACXGGvmo8xz3QYDV_O2mR5c3uwVuDtc2VLKQ9pMq4vR8130_assertion description "[Mutations in the SP110 gene result in infantile onset of the autosomal recessive primary immunodeficiency disease veno-occlusive disease with immunodeficiency syndrome (VODI), which is characterized by hypogammaglobulinemia, T-cell dysfunction, and a high frequency of hepatic veno-occlusive disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP632347.RACXGGvmo8xz3QYDV_O2mR5c3uwVuDtc2VLKQ9pMq4vR8130_provenance.
• NP984662.RA3_ulrDqmgjsKAI_Q9NytYhV-1WKJULcjBT4z7RNtods130_assertion description "[Mutations in the SP110 gene result in infantile onset of the autosomal recessive primary immunodeficiency disease veno-occlusive disease with immunodeficiency syndrome (VODI), which is characterized by hypogammaglobulinemia, T-cell dysfunction, and a high frequency of hepatic veno-occlusive disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP984662.RA3_ulrDqmgjsKAI_Q9NytYhV-1WKJULcjBT4z7RNtods130_provenance.
• NP476100.RAHHcwgz7IKkOmtshP1mW4YUGD6DIZ-5vFky4-pWGX7Gs130_assertion description "[Mutations in the SP110 gene result in infantile onset of the autosomal recessive primary immunodeficiency disease veno-occlusive disease with immunodeficiency syndrome (VODI), which is characterized by hypogammaglobulinemia, T-cell dysfunction, and a high frequency of hepatic veno-occlusive disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP476100.RAHHcwgz7IKkOmtshP1mW4YUGD6DIZ-5vFky4-pWGX7Gs130_provenance.
• assertion description "[Mutations in the SP110 gene result in infantile onset of the autosomal recessive primary immunodeficiency disease veno-occlusive disease with immunodeficiency syndrome (VODI), which is characterized by hypogammaglobulinemia, T-cell dysfunction, and a high frequency of hepatic veno-occlusive disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Mutations in the SP110 gene result in infantile onset of the autosomal recessive primary immunodeficiency disease veno-occlusive disease with immunodeficiency syndrome (VODI), which is characterized by hypogammaglobulinemia, T-cell dysfunction, and a high frequency of hepatic veno-occlusive disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP984661.RAqqSBOML3t2y9DBeRyWbYjcdpge_livEXrVLc8M-yWN8130_assertion description "[Mutations in the SP110 gene result in infantile onset of the autosomal recessive primary immunodeficiency disease veno-occlusive disease with immunodeficiency syndrome (VODI), which is characterized by hypogammaglobulinemia, T-cell dysfunction, and a high frequency of hepatic veno-occlusive disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP984661.RAqqSBOML3t2y9DBeRyWbYjcdpge_livEXrVLc8M-yWN8130_provenance.