Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1089457.RARSc7jFgMB8THTRuNfaIv1v8RcQsfpkMkU12hUNXvGyw130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1089457.RARSc7jFgMB8THTRuNfaIv1v8RcQsfpkMkU12hUNXvGyw130_assertion type Assertion NP1089457.RARSc7jFgMB8THTRuNfaIv1v8RcQsfpkMkU12hUNXvGyw130_head.
- NP1089457.RARSc7jFgMB8THTRuNfaIv1v8RcQsfpkMkU12hUNXvGyw130_assertion description "[The vascular disorder Hereditary Hemorrhagic Telangiectasia (HHT) is in general an inherited disease caused by mutations in the TGF-?/BMP receptors endoglin or ALK1 or in rare cases by mutations of the TGF-? signal transducer protein Smad4 leading to the combined syndrome of juvenile polyposis and HHT.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1089457.RARSc7jFgMB8THTRuNfaIv1v8RcQsfpkMkU12hUNXvGyw130_provenance.
- NP1089457.RARSc7jFgMB8THTRuNfaIv1v8RcQsfpkMkU12hUNXvGyw130_assertion evidence source_evidence_literature NP1089457.RARSc7jFgMB8THTRuNfaIv1v8RcQsfpkMkU12hUNXvGyw130_provenance.
- NP1089457.RARSc7jFgMB8THTRuNfaIv1v8RcQsfpkMkU12hUNXvGyw130_assertion SIO_000772 23805858 NP1089457.RARSc7jFgMB8THTRuNfaIv1v8RcQsfpkMkU12hUNXvGyw130_provenance.
- NP1089457.RARSc7jFgMB8THTRuNfaIv1v8RcQsfpkMkU12hUNXvGyw130_assertion wasDerivedFrom befree-2016 NP1089457.RARSc7jFgMB8THTRuNfaIv1v8RcQsfpkMkU12hUNXvGyw130_provenance.
- NP1089457.RARSc7jFgMB8THTRuNfaIv1v8RcQsfpkMkU12hUNXvGyw130_assertion wasGeneratedBy ECO_0000203 NP1089457.RARSc7jFgMB8THTRuNfaIv1v8RcQsfpkMkU12hUNXvGyw130_provenance.