Matches in Nanopublications for { ?s ?p "[Hereditary hemorrhagic telangiectasia (HHT) is a genetically heterogeneous vascular dysplasia with multiple telangiectases and arteriovenous malformations and it is caused by mutations in endoglin gene (ENG) (HHT1) and activin A receptor type II-like 1 gene (ACVRL1) (HHT2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP666561.RACxxg9JMALew13SzVV1aTAcKv_N9OslEO9iTtAOIKI6o130_assertion description "[Hereditary hemorrhagic telangiectasia (HHT) is a genetically heterogeneous vascular dysplasia with multiple telangiectases and arteriovenous malformations and it is caused by mutations in endoglin gene (ENG) (HHT1) and activin A receptor type II-like 1 gene (ACVRL1) (HHT2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP666561.RACxxg9JMALew13SzVV1aTAcKv_N9OslEO9iTtAOIKI6o130_provenance.
- NP176648.RAybyUuOhvTRGnrdotNTqw_YRknhf7Z3sIc-YQ5FnscO8130_assertion description "[Hereditary hemorrhagic telangiectasia (HHT) is a genetically heterogeneous vascular dysplasia with multiple telangiectases and arteriovenous malformations and it is caused by mutations in endoglin gene (ENG) (HHT1) and activin A receptor type II-like 1 gene (ACVRL1) (HHT2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP176648.RAybyUuOhvTRGnrdotNTqw_YRknhf7Z3sIc-YQ5FnscO8130_provenance.
- NP535450.RA_4M7Tsw07wHE8TM_Iv0-By9VwVCYVCn9XQ5PkKBV9lE130_assertion description "[Hereditary hemorrhagic telangiectasia (HHT) is a genetically heterogeneous vascular dysplasia with multiple telangiectases and arteriovenous malformations and it is caused by mutations in endoglin gene (ENG) (HHT1) and activin A receptor type II-like 1 gene (ACVRL1) (HHT2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP535450.RA_4M7Tsw07wHE8TM_Iv0-By9VwVCYVCn9XQ5PkKBV9lE130_provenance.
- NP535452.RA3dNznsHPEvngchv61Kzb8FRvTQ8hqQpBvyjcQgW8DCY130_assertion description "[Hereditary hemorrhagic telangiectasia (HHT) is a genetically heterogeneous vascular dysplasia with multiple telangiectases and arteriovenous malformations and it is caused by mutations in endoglin gene (ENG) (HHT1) and activin A receptor type II-like 1 gene (ACVRL1) (HHT2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP535452.RA3dNznsHPEvngchv61Kzb8FRvTQ8hqQpBvyjcQgW8DCY130_provenance.
- NP535449.RARdxLhKJ3WIiqRnMDE2UzZzLFfQfS7h7IAPUkVFWaRUI130_assertion description "[Hereditary hemorrhagic telangiectasia (HHT) is a genetically heterogeneous vascular dysplasia with multiple telangiectases and arteriovenous malformations and it is caused by mutations in endoglin gene (ENG) (HHT1) and activin A receptor type II-like 1 gene (ACVRL1) (HHT2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP535449.RARdxLhKJ3WIiqRnMDE2UzZzLFfQfS7h7IAPUkVFWaRUI130_provenance.
- NP374626.RAl8Ay5YK3wNZ9t0oljDOWECEt3tmfu9lOU1MVUVV245c130_assertion description "[Hereditary hemorrhagic telangiectasia (HHT) is a genetically heterogeneous vascular dysplasia with multiple telangiectases and arteriovenous malformations and it is caused by mutations in endoglin gene (ENG) (HHT1) and activin A receptor type II-like 1 gene (ACVRL1) (HHT2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP374626.RAl8Ay5YK3wNZ9t0oljDOWECEt3tmfu9lOU1MVUVV245c130_provenance.
- NP374820.RAo8uImuE-UwbZhXcfFzqFgGhfQRFE5tFgCesxkDuW7TY130_assertion description "[Hereditary hemorrhagic telangiectasia (HHT) is a genetically heterogeneous vascular dysplasia with multiple telangiectases and arteriovenous malformations and it is caused by mutations in endoglin gene (ENG) (HHT1) and activin A receptor type II-like 1 gene (ACVRL1) (HHT2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP374820.RAo8uImuE-UwbZhXcfFzqFgGhfQRFE5tFgCesxkDuW7TY130_provenance.
- NP535451.RAlfpIlE3NQ74O6TIWWwqCE9HkDPL4cWXYEkaykWps680130_assertion description "[Hereditary hemorrhagic telangiectasia (HHT) is a genetically heterogeneous vascular dysplasia with multiple telangiectases and arteriovenous malformations and it is caused by mutations in endoglin gene (ENG) (HHT1) and activin A receptor type II-like 1 gene (ACVRL1) (HHT2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP535451.RAlfpIlE3NQ74O6TIWWwqCE9HkDPL4cWXYEkaykWps680130_provenance.