Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP734062.RAm-hcnvSw_lgkWTkYouu82MdhidlNL_mnbaGXq03RfTA130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP734062.RAm-hcnvSw_lgkWTkYouu82MdhidlNL_mnbaGXq03RfTA130_assertion type Assertion NP734062.RAm-hcnvSw_lgkWTkYouu82MdhidlNL_mnbaGXq03RfTA130_head.
- NP734062.RAm-hcnvSw_lgkWTkYouu82MdhidlNL_mnbaGXq03RfTA130_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." NP734062.RAm-hcnvSw_lgkWTkYouu82MdhidlNL_mnbaGXq03RfTA130_provenance.
- NP734062.RAm-hcnvSw_lgkWTkYouu82MdhidlNL_mnbaGXq03RfTA130_assertion evidence source_evidence_literature NP734062.RAm-hcnvSw_lgkWTkYouu82MdhidlNL_mnbaGXq03RfTA130_provenance.
- NP734062.RAm-hcnvSw_lgkWTkYouu82MdhidlNL_mnbaGXq03RfTA130_assertion SIO_000772 18283546 NP734062.RAm-hcnvSw_lgkWTkYouu82MdhidlNL_mnbaGXq03RfTA130_provenance.
- NP734062.RAm-hcnvSw_lgkWTkYouu82MdhidlNL_mnbaGXq03RfTA130_assertion wasDerivedFrom befree-20150227 NP734062.RAm-hcnvSw_lgkWTkYouu82MdhidlNL_mnbaGXq03RfTA130_provenance.
- NP734062.RAm-hcnvSw_lgkWTkYouu82MdhidlNL_mnbaGXq03RfTA130_assertion wasGeneratedBy ECO_0000203 NP734062.RAm-hcnvSw_lgkWTkYouu82MdhidlNL_mnbaGXq03RfTA130_provenance.