Matches in Nanopublications for { ?s ?p "[A questionnaire based study provides evidence that the hereditary hemorrhagic telangiectasia (HHT) phenotype caused by mutations in endoglin (HHT1) is distinct from, and more severe than, HHT caused by mutations in ALK1 (HHT2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[A questionnaire based study provides evidence that the hereditary hemorrhagic telangiectasia (HHT) phenotype caused by mutations in endoglin (HHT1) is distinct from, and more severe than, HHT caused by mutations in ALK1 (HHT2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP215824.RAWCiOwIsnifELLAC51NMnQD0jUdzS3p_N_tm4RDuWxtc130_assertion description "[A questionnaire based study provides evidence that the hereditary hemorrhagic telangiectasia (HHT) phenotype caused by mutations in endoglin (HHT1) is distinct from, and more severe than, HHT caused by mutations in ALK1 (HHT2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP215824.RAWCiOwIsnifELLAC51NMnQD0jUdzS3p_N_tm4RDuWxtc130_provenance.
- NP201046.RAw68XeYJ7OzoinVXgTTqrpPnEdBI1IUtOIpT4v0bXuM0130_assertion description "[A questionnaire based study provides evidence that the hereditary hemorrhagic telangiectasia (HHT) phenotype caused by mutations in endoglin (HHT1) is distinct from, and more severe than, HHT caused by mutations in ALK1 (HHT2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP201046.RAw68XeYJ7OzoinVXgTTqrpPnEdBI1IUtOIpT4v0bXuM0130_provenance.