Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP689165.RAnz4R9Q_9hucaJYfx3l9SDHrIU6R4gFLD_VlNSeXMyEw130_assertion> ?p ?o ?g. }
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- NP689165.RAnz4R9Q_9hucaJYfx3l9SDHrIU6R4gFLD_VlNSeXMyEw130_assertion type Assertion NP689165.RAnz4R9Q_9hucaJYfx3l9SDHrIU6R4gFLD_VlNSeXMyEw130_head.
- NP689165.RAnz4R9Q_9hucaJYfx3l9SDHrIU6R4gFLD_VlNSeXMyEw130_assertion wasGeneratedBy ECO_0000203 NP689165.RAnz4R9Q_9hucaJYfx3l9SDHrIU6R4gFLD_VlNSeXMyEw130_provenance.
- NP689165.RAnz4R9Q_9hucaJYfx3l9SDHrIU6R4gFLD_VlNSeXMyEw130_assertion wasDerivedFrom befree-2016 NP689165.RAnz4R9Q_9hucaJYfx3l9SDHrIU6R4gFLD_VlNSeXMyEw130_provenance.
- NP689165.RAnz4R9Q_9hucaJYfx3l9SDHrIU6R4gFLD_VlNSeXMyEw130_assertion SIO_000772 18721526 NP689165.RAnz4R9Q_9hucaJYfx3l9SDHrIU6R4gFLD_VlNSeXMyEw130_provenance.
- NP689165.RAnz4R9Q_9hucaJYfx3l9SDHrIU6R4gFLD_VlNSeXMyEw130_assertion evidence source_evidence_literature NP689165.RAnz4R9Q_9hucaJYfx3l9SDHrIU6R4gFLD_VlNSeXMyEw130_provenance.
- NP689165.RAnz4R9Q_9hucaJYfx3l9SDHrIU6R4gFLD_VlNSeXMyEw130_assertion description "[Mutations in the genes encoding transforming growth factor-beta receptor types I and II (TGFBR1 and TGFBR2, respectively) are commonly identified in patients with Loeys-Dietz syndrome, as well as some patients with Marfan's syndrome or familial thoracic aortic aneurysms and dissections.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP689165.RAnz4R9Q_9hucaJYfx3l9SDHrIU6R4gFLD_VlNSeXMyEw130_provenance.