Matches in Nanopublications for { ?s ?p "[genes causing hereditary hemorrhagic telangiectasia (HHT), i.e.endoglin (ENG) and activin receptor-like kinase 1 (ACVRL1), have a relatively high mutation rate.all the four ENG mutations and one of the ACVRL1 mutations were new]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[genes causing hereditary hemorrhagic telangiectasia (HHT), i.e.endoglin (ENG) and activin receptor-like kinase 1 (ACVRL1), have a relatively high mutation rate.all the four ENG mutations and one of the ACVRL1 mutations were new]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP215831.RAMsGlotfz-AY6-s5edSXKDRuqOh2eXMRq7jxERS64dLY130_assertion description "[genes causing hereditary hemorrhagic telangiectasia (HHT), i.e.endoglin (ENG) and activin receptor-like kinase 1 (ACVRL1), have a relatively high mutation rate.all the four ENG mutations and one of the ACVRL1 mutations were new]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP215831.RAMsGlotfz-AY6-s5edSXKDRuqOh2eXMRq7jxERS64dLY130_provenance.