Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP535422.RAmf33Ppg0NSoqGxVjRWzDibDyLgGncUiaMp7aHjQACqI130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP535422.RAmf33Ppg0NSoqGxVjRWzDibDyLgGncUiaMp7aHjQACqI130_assertion type Assertion NP535422.RAmf33Ppg0NSoqGxVjRWzDibDyLgGncUiaMp7aHjQACqI130_head.
- NP535422.RAmf33Ppg0NSoqGxVjRWzDibDyLgGncUiaMp7aHjQACqI130_assertion description "[Hereditary hemorrhagic telangiectasia (HHT) is an autosomal dominant and age-dependent vascular disorder originated by mutations in Endoglin (ENG) or activin receptor-like kinase-1 (ALK1, ACVRL1) genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP535422.RAmf33Ppg0NSoqGxVjRWzDibDyLgGncUiaMp7aHjQACqI130_provenance.
- NP535422.RAmf33Ppg0NSoqGxVjRWzDibDyLgGncUiaMp7aHjQACqI130_assertion evidence source_evidence_literature NP535422.RAmf33Ppg0NSoqGxVjRWzDibDyLgGncUiaMp7aHjQACqI130_provenance.
- NP535422.RAmf33Ppg0NSoqGxVjRWzDibDyLgGncUiaMp7aHjQACqI130_assertion SIO_000772 16470589 NP535422.RAmf33Ppg0NSoqGxVjRWzDibDyLgGncUiaMp7aHjQACqI130_provenance.
- NP535422.RAmf33Ppg0NSoqGxVjRWzDibDyLgGncUiaMp7aHjQACqI130_assertion wasDerivedFrom befree-2016 NP535422.RAmf33Ppg0NSoqGxVjRWzDibDyLgGncUiaMp7aHjQACqI130_provenance.
- NP535422.RAmf33Ppg0NSoqGxVjRWzDibDyLgGncUiaMp7aHjQACqI130_assertion wasGeneratedBy ECO_0000203 NP535422.RAmf33Ppg0NSoqGxVjRWzDibDyLgGncUiaMp7aHjQACqI130_provenance.