Matches in Nanopublications for { ?s ?p "[Hereditary hemorrhagic telangiectasia (HHT) is an autosomal dominant and age-dependent vascular disorder originated by mutations in Endoglin (ENG) or activin receptor-like kinase-1 (ALK1, ACVRL1) genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[Hereditary hemorrhagic telangiectasia (HHT) is an autosomal dominant and age-dependent vascular disorder originated by mutations in Endoglin (ENG) or activin receptor-like kinase-1 (ALK1, ACVRL1) genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP606066.RAfG8m9I-IMKUlZBo11dY7IVOIJ4oHrS57-ceOYkOmYnc130_assertion description "[Hereditary hemorrhagic telangiectasia (HHT) is an autosomal dominant and age-dependent vascular disorder originated by mutations in Endoglin (ENG) or activin receptor-like kinase-1 (ALK1, ACVRL1) genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP606066.RAfG8m9I-IMKUlZBo11dY7IVOIJ4oHrS57-ceOYkOmYnc130_provenance.
- NP469104.RAdjY8n1jByABc8zwujS3mlIGKOx6_1Si5-nOmLyaVQjE130_assertion description "[Hereditary hemorrhagic telangiectasia (HHT) is an autosomal dominant and age-dependent vascular disorder originated by mutations in Endoglin (ENG) or activin receptor-like kinase-1 (ALK1, ACVRL1) genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP469104.RAdjY8n1jByABc8zwujS3mlIGKOx6_1Si5-nOmLyaVQjE130_provenance.
- assertion description "[Hereditary hemorrhagic telangiectasia (HHT) is an autosomal dominant and age-dependent vascular disorder originated by mutations in Endoglin (ENG) or activin receptor-like kinase-1 (ALK1, ACVRL1) genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP374773.RAXKpFesZqxWFUJeSrK1yXcQXxtDh3jOtkJwebD9SUajs130_assertion description "[Hereditary hemorrhagic telangiectasia (HHT) is an autosomal dominant and age-dependent vascular disorder originated by mutations in Endoglin (ENG) or activin receptor-like kinase-1 (ALK1, ACVRL1) genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP374773.RAXKpFesZqxWFUJeSrK1yXcQXxtDh3jOtkJwebD9SUajs130_provenance.
- NP852946.RAKleQH0bjHBUqS-hOxZ6dEHSxi-dGjv0sgzrr7aaq7JA130_assertion description "[Hereditary hemorrhagic telangiectasia (HHT) is an autosomal dominant and age-dependent vascular disorder originated by mutations in Endoglin (ENG) or activin receptor-like kinase-1 (ALK1, ACVRL1) genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP852946.RAKleQH0bjHBUqS-hOxZ6dEHSxi-dGjv0sgzrr7aaq7JA130_provenance.
- NP535422.RAmf33Ppg0NSoqGxVjRWzDibDyLgGncUiaMp7aHjQACqI130_assertion description "[Hereditary hemorrhagic telangiectasia (HHT) is an autosomal dominant and age-dependent vascular disorder originated by mutations in Endoglin (ENG) or activin receptor-like kinase-1 (ALK1, ACVRL1) genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP535422.RAmf33Ppg0NSoqGxVjRWzDibDyLgGncUiaMp7aHjQACqI130_provenance.