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- NP222412.RAGuORbTRXC24stuqRWPLtrTIPQWhw9zmpNhJDCjieAWg130_assertion type Assertion NP222412.RAGuORbTRXC24stuqRWPLtrTIPQWhw9zmpNhJDCjieAWg130_head.
- NP222412.RAGuORbTRXC24stuqRWPLtrTIPQWhw9zmpNhJDCjieAWg130_assertion wasGeneratedBy ECO_0000203 NP222412.RAGuORbTRXC24stuqRWPLtrTIPQWhw9zmpNhJDCjieAWg130_provenance.
- NP222412.RAGuORbTRXC24stuqRWPLtrTIPQWhw9zmpNhJDCjieAWg130_assertion wasDerivedFrom befree-20150227 NP222412.RAGuORbTRXC24stuqRWPLtrTIPQWhw9zmpNhJDCjieAWg130_provenance.
- NP222412.RAGuORbTRXC24stuqRWPLtrTIPQWhw9zmpNhJDCjieAWg130_assertion SIO_000772 19508727 NP222412.RAGuORbTRXC24stuqRWPLtrTIPQWhw9zmpNhJDCjieAWg130_provenance.
- NP222412.RAGuORbTRXC24stuqRWPLtrTIPQWhw9zmpNhJDCjieAWg130_assertion evidence source_evidence_literature NP222412.RAGuORbTRXC24stuqRWPLtrTIPQWhw9zmpNhJDCjieAWg130_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.