Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP544036.RAc8Ln6mPPtjMjyB1dK_h56SUXBqpaAaNRSS0JwYePWP0130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP544036.RAc8Ln6mPPtjMjyB1dK_h56SUXBqpaAaNRSS0JwYePWP0130_assertion type Assertion NP544036.RAc8Ln6mPPtjMjyB1dK_h56SUXBqpaAaNRSS0JwYePWP0130_head.
- NP544036.RAc8Ln6mPPtjMjyB1dK_h56SUXBqpaAaNRSS0JwYePWP0130_assertion description "[Hereditary hemorrhagic telangiectasia (HHT), the most common inherited vascular disorder, is caused by mutations in genes involved in�the transforming growth factor beta (TGF-?) signaling pathway (ENG, ACVRL1, and SMAD4).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP544036.RAc8Ln6mPPtjMjyB1dK_h56SUXBqpaAaNRSS0JwYePWP0130_provenance.
- NP544036.RAc8Ln6mPPtjMjyB1dK_h56SUXBqpaAaNRSS0JwYePWP0130_assertion evidence source_evidence_literature NP544036.RAc8Ln6mPPtjMjyB1dK_h56SUXBqpaAaNRSS0JwYePWP0130_provenance.
- NP544036.RAc8Ln6mPPtjMjyB1dK_h56SUXBqpaAaNRSS0JwYePWP0130_assertion SIO_000772 23972370 NP544036.RAc8Ln6mPPtjMjyB1dK_h56SUXBqpaAaNRSS0JwYePWP0130_provenance.
- NP544036.RAc8Ln6mPPtjMjyB1dK_h56SUXBqpaAaNRSS0JwYePWP0130_assertion wasDerivedFrom befree-20150227 NP544036.RAc8Ln6mPPtjMjyB1dK_h56SUXBqpaAaNRSS0JwYePWP0130_provenance.
- NP544036.RAc8Ln6mPPtjMjyB1dK_h56SUXBqpaAaNRSS0JwYePWP0130_assertion wasGeneratedBy ECO_0000203 NP544036.RAc8Ln6mPPtjMjyB1dK_h56SUXBqpaAaNRSS0JwYePWP0130_provenance.