Matches in Nanopublications for { ?s ?p "[Abetalipoproteinemia (ABL) is an inherited disease characterized by the defective assembly and secretion of apolipoprotein B-containing lipoproteins caused by mutations in the microsomal triglyceride transfer protein large subunit (MTP) gene (MTTP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP724008.RAbyza47L2ES0ffnTC_la5pxWDlp7o3bXK7iCOJMMHb7A130_assertion description "[Abetalipoproteinemia (ABL) is an inherited disease characterized by the defective assembly and secretion of apolipoprotein B-containing lipoproteins caused by mutations in the microsomal triglyceride transfer protein large subunit (MTP) gene (MTTP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP724008.RAbyza47L2ES0ffnTC_la5pxWDlp7o3bXK7iCOJMMHb7A130_provenance.
- assertion description "[Abetalipoproteinemia (ABL) is an inherited disease characterized by the defective assembly and secretion of apolipoprotein B-containing lipoproteins caused by mutations in the microsomal triglyceride transfer protein large subunit (MTP) gene (MTTP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP422528.RAJUEvcPTww6CHaz2bXWt94DtVidLhbxBF4Pu-h_XlV8Y130_assertion description "[Abetalipoproteinemia (ABL) is an inherited disease characterized by the defective assembly and secretion of apolipoprotein B-containing lipoproteins caused by mutations in the microsomal triglyceride transfer protein large subunit (MTP) gene (MTTP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP422528.RAJUEvcPTww6CHaz2bXWt94DtVidLhbxBF4Pu-h_XlV8Y130_provenance.
- NP438273.RAYVddYlwI89JQyO-_y1aSqdXPrrYCcXR6fJU_KfNUKV4130_assertion description "[Abetalipoproteinemia (ABL) is an inherited disease characterized by the defective assembly and secretion of apolipoprotein B-containing lipoproteins caused by mutations in the microsomal triglyceride transfer protein large subunit (MTP) gene (MTTP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP438273.RAYVddYlwI89JQyO-_y1aSqdXPrrYCcXR6fJU_KfNUKV4130_provenance.
- NP243734.RAoaFW0jYUFhJc0xs4zovPeddkXikOV-i2uH64lbcG7ms130_assertion description "[Abetalipoproteinemia (ABL) is an inherited disease characterized by the defective assembly and secretion of apolipoprotein B-containing lipoproteins caused by mutations in the microsomal triglyceride transfer protein large subunit (MTP) gene (MTTP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP243734.RAoaFW0jYUFhJc0xs4zovPeddkXikOV-i2uH64lbcG7ms130_provenance.
- NP952440.RAnY1x2NuPsPua9zDaYr9_OwhUMv-g2dZuOBZzY_hjqgg130_assertion description "[Abetalipoproteinemia (ABL) is an inherited disease characterized by the defective assembly and secretion of apolipoprotein B-containing lipoproteins caused by mutations in the microsomal triglyceride transfer protein large subunit (MTP) gene (MTTP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP952440.RAnY1x2NuPsPua9zDaYr9_OwhUMv-g2dZuOBZzY_hjqgg130_provenance.
- NP243870.RA7RX8sj_wL7PlayK_f2NKN28qT-ZdiaUgnHRO94YErzY130_assertion description "[Abetalipoproteinemia (ABL) is an inherited disease characterized by the defective assembly and secretion of apolipoprotein B-containing lipoproteins caused by mutations in the microsomal triglyceride transfer protein large subunit (MTP) gene (MTTP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP243870.RA7RX8sj_wL7PlayK_f2NKN28qT-ZdiaUgnHRO94YErzY130_provenance.
- NP576893.RA68R5MTZJWURA0XLczKCFb5s5Ro2cmy2S6OCQJIgM4Uc130_assertion description "[Abetalipoproteinemia (ABL) is an inherited disease characterized by the defective assembly and secretion of apolipoprotein B-containing lipoproteins caused by mutations in the microsomal triglyceride transfer protein large subunit (MTP) gene (MTTP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP576893.RA68R5MTZJWURA0XLczKCFb5s5Ro2cmy2S6OCQJIgM4Uc130_provenance.