Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP535449.RARdxLhKJ3WIiqRnMDE2UzZzLFfQfS7h7IAPUkVFWaRUI130_assertion> ?p ?o ?g. }
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- NP535449.RARdxLhKJ3WIiqRnMDE2UzZzLFfQfS7h7IAPUkVFWaRUI130_assertion type Assertion NP535449.RARdxLhKJ3WIiqRnMDE2UzZzLFfQfS7h7IAPUkVFWaRUI130_head.
- NP535449.RARdxLhKJ3WIiqRnMDE2UzZzLFfQfS7h7IAPUkVFWaRUI130_assertion wasGeneratedBy ECO_0000203 NP535449.RARdxLhKJ3WIiqRnMDE2UzZzLFfQfS7h7IAPUkVFWaRUI130_provenance.
- NP535449.RARdxLhKJ3WIiqRnMDE2UzZzLFfQfS7h7IAPUkVFWaRUI130_assertion wasDerivedFrom befree-2016 NP535449.RARdxLhKJ3WIiqRnMDE2UzZzLFfQfS7h7IAPUkVFWaRUI130_provenance.
- NP535449.RARdxLhKJ3WIiqRnMDE2UzZzLFfQfS7h7IAPUkVFWaRUI130_assertion SIO_000772 16470787 NP535449.RARdxLhKJ3WIiqRnMDE2UzZzLFfQfS7h7IAPUkVFWaRUI130_provenance.
- NP535449.RARdxLhKJ3WIiqRnMDE2UzZzLFfQfS7h7IAPUkVFWaRUI130_assertion evidence source_evidence_literature NP535449.RARdxLhKJ3WIiqRnMDE2UzZzLFfQfS7h7IAPUkVFWaRUI130_provenance.
- NP535449.RARdxLhKJ3WIiqRnMDE2UzZzLFfQfS7h7IAPUkVFWaRUI130_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." NP535449.RARdxLhKJ3WIiqRnMDE2UzZzLFfQfS7h7IAPUkVFWaRUI130_provenance.