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Matches in Nanopublications for { ?s ?p "[An analysis of the genotype-phenotype correlation is consistent with a more common 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. }

• assertion description "[An analysis of the genotype-phenotype correlation is consistent with a more common 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." provenance.
• assertion description "[An analysis of the genotype-phenotype correlation is consistent with a more common 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." provenance.
• assertion description "[An analysis of the genotype-phenotype correlation is consistent with a more common 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." provenance.
• NP266311.RAbMgMDxnU-vzMbT3DjFAoU2O53b5oZQOM-PbRm4KLX0I130_assertion description "[An analysis of the genotype-phenotype correlation is consistent with a more common 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." NP266311.RAbMgMDxnU-vzMbT3DjFAoU2O53b5oZQOM-PbRm4KLX0I130_provenance.
• NP149459.RAVAwuN5XipFy0ZkKnMNB4gvhxd-vwfHBEP31ma_dsjyg130_assertion description "[An analysis of the genotype-phenotype correlation is consistent with a more common 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." NP149459.RAVAwuN5XipFy0ZkKnMNB4gvhxd-vwfHBEP31ma_dsjyg130_provenance.
• NP149461.RAvpCdzNrcU4HXkMqez655C6oCMa1aG1pneMdMYStqf8Q130_assertion description "[An analysis of the genotype-phenotype correlation is consistent with a more common 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." NP149461.RAvpCdzNrcU4HXkMqez655C6oCMa1aG1pneMdMYStqf8Q130_provenance.
• NP291963.RAxrhzfRGgyog2nd09KKDe5QzbZuVBYUIrnf2YcLiYm-E130_assertion description "[An analysis of the genotype-phenotype correlation is consistent with a more common 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." NP291963.RAxrhzfRGgyog2nd09KKDe5QzbZuVBYUIrnf2YcLiYm-E130_provenance.
• NP186855.RAHRG02ukFw0GwyOsgpOcxfIJdT-f9gPf7aCk_kntQjes130_assertion description "[An analysis of the genotype-phenotype correlation is consistent with a more common 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." NP186855.RAHRG02ukFw0GwyOsgpOcxfIJdT-f9gPf7aCk_kntQjes130_provenance.
• assertion description "[An analysis of the genotype-phenotype correlation is consistent with a more common 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." provenance.
• assertion description "[An analysis of the genotype-phenotype correlation is consistent with a more common 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." provenance.
• assertion description "[An analysis of the genotype-phenotype correlation is consistent with a more common 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." provenance.
• NP212583.RATYz8FBdDbKXuZs8-xVCXby3IpaxjlAWkCdkV02wd4-k130_assertion description "[An analysis of the genotype-phenotype correlation is consistent with a more common 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." NP212583.RATYz8FBdDbKXuZs8-xVCXby3IpaxjlAWkCdkV02wd4-k130_provenance.
• NP212585.RAbWvWsG2ILDyL6CptIpV-dRRuksBl6S5mV2iL-0ilRE0130_assertion description "[An analysis of the genotype-phenotype correlation is consistent with a more common 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." NP212585.RAbWvWsG2ILDyL6CptIpV-dRRuksBl6S5mV2iL-0ilRE0130_provenance.
• NP216143.RAabdH0-vizb_jK-OtZX7O8HPya6UPyEIP9Znl6ja1Ub4130_assertion description "[An analysis of the genotype-phenotype correlation is consistent with a more common 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." NP216143.RAabdH0-vizb_jK-OtZX7O8HPya6UPyEIP9Znl6ja1Ub4130_provenance.
• NP540688.RAbJcy5M8qMnKNHrTPUR_boRwGpsPa5fW3a0YP7UIQeOA130_assertion description "[An analysis of the genotype-phenotype correlation is consistent with a more common 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." NP540688.RAbJcy5M8qMnKNHrTPUR_boRwGpsPa5fW3a0YP7UIQeOA130_provenance.
• NP540687.RAC3txjM_dEc3cxmYT2NW6FNhrpeZWcIMNfdDy0j6or_s130_assertion description "[An analysis of the genotype-phenotype correlation is consistent with a more common 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." NP540687.RAC3txjM_dEc3cxmYT2NW6FNhrpeZWcIMNfdDy0j6or_s130_provenance.
• NP216142.RAGCLabsdAoHxgXWYJ4CUGOddvYnr3zWC8L_gMV7f2Fko130_assertion description "[An analysis of the genotype-phenotype correlation is consistent with a more common 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." NP216142.RAGCLabsdAoHxgXWYJ4CUGOddvYnr3zWC8L_gMV7f2Fko130_provenance.
• NP540686.RAL0nw2Rd-XtTPkVEKfIM-6s0zBJNiiFxs6SfJmypCWiY130_assertion description "[An analysis of the genotype-phenotype correlation is consistent with a more common 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." NP540686.RAL0nw2Rd-XtTPkVEKfIM-6s0zBJNiiFxs6SfJmypCWiY130_provenance.
• NP540689.RA-zbyhG31cFegIshysrH9lg9cs7yhWgMwxiu72mvuHXo130_assertion description "[An analysis of the genotype-phenotype correlation is consistent with a more common 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." NP540689.RA-zbyhG31cFegIshysrH9lg9cs7yhWgMwxiu72mvuHXo130_provenance.