Matches in Nanopublications for { ?s ?p "[Our questionnaire based study provides evidence that the 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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- NP45108.RAVuLK_9j7cG2pS385Zw3bltUyVutvulQOgUaST511Bm0130_assertion description "[Our questionnaire based study provides evidence that the 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." NP45108.RAVuLK_9j7cG2pS385Zw3bltUyVutvulQOgUaST511Bm0130_provenance.
- assertion description "[Our questionnaire based study provides evidence that the 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.
- NP49326.RAQXv6bbVmc84IxurtlVVqlfdf_TRVstrou30nRZy0F-M130_assertion description "[Our questionnaire based study provides evidence that the 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." NP49326.RAQXv6bbVmc84IxurtlVVqlfdf_TRVstrou30nRZy0F-M130_provenance.