Matches in Nanopublications for { ?s ?p "[These results demonstrate the importance of ACVRL1 and ENG mutations in German hereditary hemorrhagic telangiectasia (HHT) patients displaying mutation frequencies over 80%.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[These results demonstrate the importance of ACVRL1 and ENG mutations in German hereditary hemorrhagic telangiectasia (HHT) patients displaying mutation frequencies over 80%.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP152718.RAtesYcMNLoN5-ByfuuVZyoRgqR0tH9N5dS9rfY6-ngmI130_assertion description "[These results demonstrate the importance of ACVRL1 and ENG mutations in German hereditary hemorrhagic telangiectasia (HHT) patients displaying mutation frequencies over 80%.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP152718.RAtesYcMNLoN5-ByfuuVZyoRgqR0tH9N5dS9rfY6-ngmI130_provenance.
- NP152709.RA8sdulOew4J0moFarUa7xapdHjk2YTGGVLp2zNpm08IA130_assertion description "[These results demonstrate the importance of ACVRL1 and ENG mutations in German hereditary hemorrhagic telangiectasia (HHT) patients displaying mutation frequencies over 80%.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP152709.RA8sdulOew4J0moFarUa7xapdHjk2YTGGVLp2zNpm08IA130_provenance.
- assertion description "[These results demonstrate the importance of ACVRL1 and ENG mutations in German hereditary hemorrhagic telangiectasia (HHT) patients displaying mutation frequencies over 80%.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP210757.RAcLs7t0XvsiGw_04yiuk2xmSFHXp9EeBmN29-USdINII130_assertion description "[These results demonstrate the importance of ACVRL1 and ENG mutations in German hereditary hemorrhagic telangiectasia (HHT) patients displaying mutation frequencies over 80%.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP210757.RAcLs7t0XvsiGw_04yiuk2xmSFHXp9EeBmN29-USdINII130_provenance.
- NP210758.RAbD036k8TpizibzeIDL2RDxY5fU1jlkOmPQRMG_Rj9aM130_assertion description "[These results demonstrate the importance of ACVRL1 and ENG mutations in German hereditary hemorrhagic telangiectasia (HHT) patients displaying mutation frequencies over 80%.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP210758.RAbD036k8TpizibzeIDL2RDxY5fU1jlkOmPQRMG_Rj9aM130_provenance.
- NP215822.RAscdWiJXIpawtP1iI8aegPzyEybvNPgHmbxoQso8hrqI130_assertion description "[These results demonstrate the importance of ACVRL1 and ENG mutations in German hereditary hemorrhagic telangiectasia (HHT) patients displaying mutation frequencies over 80%.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP215822.RAscdWiJXIpawtP1iI8aegPzyEybvNPgHmbxoQso8hrqI130_provenance.
- NP215830.RAx2wL55ZuT9ydHQX-AoGmf601sBwLftP04F-IGiV4OxA130_assertion description "[These results demonstrate the importance of ACVRL1 and ENG mutations in German hereditary hemorrhagic telangiectasia (HHT) patients displaying mutation frequencies over 80%.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP215830.RAx2wL55ZuT9ydHQX-AoGmf601sBwLftP04F-IGiV4OxA130_provenance.