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Matches in Nanopublications for { ?s ?p "[A point mutation in ABC1 gene in a patient with severe premature coronary heart disease and mild clinical phenotype of Tangier disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP328509.RAXVEkJNuznaU6NzdVVwulKrVZXv-uVPDJwsj07448yuo130_assertion description "[A point mutation in ABC1 gene in a patient with severe premature coronary heart disease and mild clinical phenotype of Tangier disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP328509.RAXVEkJNuznaU6NzdVVwulKrVZXv-uVPDJwsj07448yuo130_provenance.
• assertion description "[A point mutation in ABC1 gene in a patient with severe premature coronary heart disease and mild clinical phenotype of Tangier disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[A point mutation in ABC1 gene in a patient with severe premature coronary heart disease and mild clinical phenotype of Tangier disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[A point mutation in ABC1 gene in a patient with severe premature coronary heart disease and mild clinical phenotype of Tangier disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[A point mutation in ABC1 gene in a patient with severe premature coronary heart disease and mild clinical phenotype of Tangier disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[A point mutation in ABC1 gene in a patient with severe premature coronary heart disease and mild clinical phenotype of Tangier disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP206389.RAWulyuMDfeUdBW9ruymmoHIcGeezW0fDHUlP5K6X3qZo130_assertion description "[A point mutation in ABC1 gene in a patient with severe premature coronary heart disease and mild clinical phenotype of Tangier disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206389.RAWulyuMDfeUdBW9ruymmoHIcGeezW0fDHUlP5K6X3qZo130_provenance.
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• assertion description "[A point mutation in ABC1 gene in a patient with severe premature coronary heart disease and mild clinical phenotype of Tangier disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[A point mutation in ABC1 gene in a patient with severe premature coronary heart disease and mild clinical phenotype of Tangier disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[A point mutation in ABC1 gene in a patient with severe premature coronary heart disease and mild clinical phenotype of Tangier disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[A point mutation in ABC1 gene in a patient with severe premature coronary heart disease and mild clinical phenotype of Tangier disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP936293.RAl02RzDOTYy1WoRGK75PkQK52k0xBJMazKuWKEkrD0Ds130_assertion description "[A point mutation in ABC1 gene in a patient with severe premature coronary heart disease and mild clinical phenotype of Tangier disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP936293.RAl02RzDOTYy1WoRGK75PkQK52k0xBJMazKuWKEkrD0Ds130_provenance.
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• NP936305.RAAvy-E-kEkPMjuL-DXKwrmlvNIJ76kPzt3-_VxzmU8sU130_assertion description "[A point mutation in ABC1 gene in a patient with severe premature coronary heart disease and mild clinical phenotype of Tangier disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP936305.RAAvy-E-kEkPMjuL-DXKwrmlvNIJ76kPzt3-_VxzmU8sU130_provenance.
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• NP311448.RAnl7NfJRmwmMBmL0T0CJHMF6a9QmpJkdKHL8YZdRuwkI130_assertion description "[A point mutation in ABC1 gene in a patient with severe premature coronary heart disease and mild clinical phenotype of Tangier disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311448.RAnl7NfJRmwmMBmL0T0CJHMF6a9QmpJkdKHL8YZdRuwkI130_provenance.
• NP936294.RAO_gadkaewLKj_2rjOERoSmHwWC_i5nM-6xjLZzBHr0A130_assertion description "[A point mutation in ABC1 gene in a patient with severe premature coronary heart disease and mild clinical phenotype of Tangier disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP936294.RAO_gadkaewLKj_2rjOERoSmHwWC_i5nM-6xjLZzBHr0A130_provenance.
• NP311449.RANyp2c3xS1ZoANUxmGJI6scw2OcII-CMUmdW4R-HNSUY130_assertion description "[A point mutation in ABC1 gene in a patient with severe premature coronary heart disease and mild clinical phenotype of Tangier disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311449.RANyp2c3xS1ZoANUxmGJI6scw2OcII-CMUmdW4R-HNSUY130_provenance.
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