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- NP656151.RAwOwU_8s1NDl8OEhU73YE16RxWHHVLXqqfZyecVlAthU130_assertion type Assertion NP656151.RAwOwU_8s1NDl8OEhU73YE16RxWHHVLXqqfZyecVlAthU130_head.
- NP656151.RAwOwU_8s1NDl8OEhU73YE16RxWHHVLXqqfZyecVlAthU130_assertion description "[Mutations in endoglin and activin receptor-like kinase 1 (ALK1), an endothelial specific TGF-beta type I receptor, have been linked to hereditary hemorrhagic telangiectasia (HHT), an autosomal dominant vascular dysplasia characterized by telangiectases and arteriovenous malformations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP656151.RAwOwU_8s1NDl8OEhU73YE16RxWHHVLXqqfZyecVlAthU130_provenance.
- NP656151.RAwOwU_8s1NDl8OEhU73YE16RxWHHVLXqqfZyecVlAthU130_assertion evidence source_evidence_literature NP656151.RAwOwU_8s1NDl8OEhU73YE16RxWHHVLXqqfZyecVlAthU130_provenance.
- NP656151.RAwOwU_8s1NDl8OEhU73YE16RxWHHVLXqqfZyecVlAthU130_assertion SIO_000772 18283546 NP656151.RAwOwU_8s1NDl8OEhU73YE16RxWHHVLXqqfZyecVlAthU130_provenance.
- NP656151.RAwOwU_8s1NDl8OEhU73YE16RxWHHVLXqqfZyecVlAthU130_assertion wasDerivedFrom befree-2016 NP656151.RAwOwU_8s1NDl8OEhU73YE16RxWHHVLXqqfZyecVlAthU130_provenance.
- NP656151.RAwOwU_8s1NDl8OEhU73YE16RxWHHVLXqqfZyecVlAthU130_assertion wasGeneratedBy ECO_0000203 NP656151.RAwOwU_8s1NDl8OEhU73YE16RxWHHVLXqqfZyecVlAthU130_provenance.