Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP333145.RAHUGxxM3-w_mNSVrfDYRVEv3g3qLKIKEYCgnTviYo8vw130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP333145.RAHUGxxM3-w_mNSVrfDYRVEv3g3qLKIKEYCgnTviYo8vw130_assertion type Assertion NP333145.RAHUGxxM3-w_mNSVrfDYRVEv3g3qLKIKEYCgnTviYo8vw130_head.
- NP333145.RAHUGxxM3-w_mNSVrfDYRVEv3g3qLKIKEYCgnTviYo8vw130_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." NP333145.RAHUGxxM3-w_mNSVrfDYRVEv3g3qLKIKEYCgnTviYo8vw130_provenance.
- NP333145.RAHUGxxM3-w_mNSVrfDYRVEv3g3qLKIKEYCgnTviYo8vw130_assertion evidence source_evidence_literature NP333145.RAHUGxxM3-w_mNSVrfDYRVEv3g3qLKIKEYCgnTviYo8vw130_provenance.
- NP333145.RAHUGxxM3-w_mNSVrfDYRVEv3g3qLKIKEYCgnTviYo8vw130_assertion SIO_000772 18283546 NP333145.RAHUGxxM3-w_mNSVrfDYRVEv3g3qLKIKEYCgnTviYo8vw130_provenance.
- NP333145.RAHUGxxM3-w_mNSVrfDYRVEv3g3qLKIKEYCgnTviYo8vw130_assertion wasDerivedFrom befree-20140225 NP333145.RAHUGxxM3-w_mNSVrfDYRVEv3g3qLKIKEYCgnTviYo8vw130_provenance.
- NP333145.RAHUGxxM3-w_mNSVrfDYRVEv3g3qLKIKEYCgnTviYo8vw130_assertion wasGeneratedBy ECO_0000203 NP333145.RAHUGxxM3-w_mNSVrfDYRVEv3g3qLKIKEYCgnTviYo8vw130_provenance.