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- NP176648.RAybyUuOhvTRGnrdotNTqw_YRknhf7Z3sIc-YQ5FnscO8130_assertion type Assertion NP176648.RAybyUuOhvTRGnrdotNTqw_YRknhf7Z3sIc-YQ5FnscO8130_head.
- NP176648.RAybyUuOhvTRGnrdotNTqw_YRknhf7Z3sIc-YQ5FnscO8130_assertion wasGeneratedBy ECO_0000203 NP176648.RAybyUuOhvTRGnrdotNTqw_YRknhf7Z3sIc-YQ5FnscO8130_provenance.
- NP176648.RAybyUuOhvTRGnrdotNTqw_YRknhf7Z3sIc-YQ5FnscO8130_assertion wasDerivedFrom befree-20140225 NP176648.RAybyUuOhvTRGnrdotNTqw_YRknhf7Z3sIc-YQ5FnscO8130_provenance.
- NP176648.RAybyUuOhvTRGnrdotNTqw_YRknhf7Z3sIc-YQ5FnscO8130_assertion SIO_000772 16470787 NP176648.RAybyUuOhvTRGnrdotNTqw_YRknhf7Z3sIc-YQ5FnscO8130_provenance.
- NP176648.RAybyUuOhvTRGnrdotNTqw_YRknhf7Z3sIc-YQ5FnscO8130_assertion evidence source_evidence_literature NP176648.RAybyUuOhvTRGnrdotNTqw_YRknhf7Z3sIc-YQ5FnscO8130_provenance.
- NP176648.RAybyUuOhvTRGnrdotNTqw_YRknhf7Z3sIc-YQ5FnscO8130_assertion description "[Hereditary hemorrhagic telangiectasia (HHT) is a genetically heterogeneous vascular dysplasia with multiple telangiectases and arteriovenous malformations and it is caused by mutations in endoglin gene (ENG) (HHT1) and activin A receptor type II-like 1 gene (ACVRL1) (HHT2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP176648.RAybyUuOhvTRGnrdotNTqw_YRknhf7Z3sIc-YQ5FnscO8130_provenance.