Matches in Nanopublications for { ?s ?p "[The genotype-phenotype correlation was consistent with a higher frequency of pulmonary arteriovenous malformations in patients with ENG mutations than in patients with ACVRL1 mutations in our collective.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP166845.RADAyQNKgQx0hj_y_fhgFhrryU_hgcS0t6PyYFSntsnoA130_assertion description "[The genotype-phenotype correlation was consistent with a higher frequency of pulmonary arteriovenous malformations in patients with ENG mutations than in patients with ACVRL1 mutations in our collective.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP166845.RADAyQNKgQx0hj_y_fhgFhrryU_hgcS0t6PyYFSntsnoA130_provenance.
- NP374827.RAXRAEBxbgKKoCAxST-rNvBe3PNVjDFqktGCrb84pzp1c130_assertion description "[The genotype-phenotype correlation was consistent with a higher frequency of pulmonary arteriovenous malformations in patients with ENG mutations than in patients with ACVRL1 mutations in our collective.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP374827.RAXRAEBxbgKKoCAxST-rNvBe3PNVjDFqktGCrb84pzp1c130_provenance.
- NP374633.RA6TXbqyCKVB4Daii3ZQ-E6Zby3Ty8MZje10B0kLC2QJg130_assertion description "[The genotype-phenotype correlation was consistent with a higher frequency of pulmonary arteriovenous malformations in patients with ENG mutations than in patients with ACVRL1 mutations in our collective.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP374633.RA6TXbqyCKVB4Daii3ZQ-E6Zby3Ty8MZje10B0kLC2QJg130_provenance.
- NP744092.RADR_ByiPvV7RkAPzNedymuOoVPmb3gMTE0uptwviNTmM130_assertion description "[The genotype-phenotype correlation was consistent with a higher frequency of pulmonary arteriovenous malformations in patients with ENG mutations than in patients with ACVRL1 mutations in our collective.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP744092.RADR_ByiPvV7RkAPzNedymuOoVPmb3gMTE0uptwviNTmM130_provenance.
- NP222315.RA7_3G1M6PKAQMpZR05nvo8VRcF6gdqb5THR6x0e9vmkE130_assertion description "[The genotype-phenotype correlation was consistent with a higher frequency of pulmonary arteriovenous malformations in patients with ENG mutations than in patients with ACVRL1 mutations in our collective.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP222315.RA7_3G1M6PKAQMpZR05nvo8VRcF6gdqb5THR6x0e9vmkE130_provenance.
- NP744089.RA1Gn4AXWe1fM1YYSz6HjZP4bIuN-rdZh2xCxKTl_koT8130_assertion description "[The genotype-phenotype correlation was consistent with a higher frequency of pulmonary arteriovenous malformations in patients with ENG mutations than in patients with ACVRL1 mutations in our collective.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP744089.RA1Gn4AXWe1fM1YYSz6HjZP4bIuN-rdZh2xCxKTl_koT8130_provenance.
- NP222412.RAGuORbTRXC24stuqRWPLtrTIPQWhw9zmpNhJDCjieAWg130_assertion description "[The genotype-phenotype correlation was consistent with a higher frequency of pulmonary arteriovenous malformations in patients with ENG mutations than in patients with ACVRL1 mutations in our collective.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP222412.RAGuORbTRXC24stuqRWPLtrTIPQWhw9zmpNhJDCjieAWg130_provenance.
- NP744091.RASYGV3MiQIshHuaugdHiHy_GDek0UvaP1nnI347TpZb8130_assertion description "[The genotype-phenotype correlation was consistent with a higher frequency of pulmonary arteriovenous malformations in patients with ENG mutations than in patients with ACVRL1 mutations in our collective.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP744091.RASYGV3MiQIshHuaugdHiHy_GDek0UvaP1nnI347TpZb8130_provenance.
- NP744093.RAjS2yjQ2gJfs5q-LnqD0KfZQzKtUnzmk0ktt0gWqPxHM130_assertion description "[The genotype-phenotype correlation was consistent with a higher frequency of pulmonary arteriovenous malformations in patients with ENG mutations than in patients with ACVRL1 mutations in our collective.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP744093.RAjS2yjQ2gJfs5q-LnqD0KfZQzKtUnzmk0ktt0gWqPxHM130_provenance.