Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1022862.RAHkm1WnXAuk2BsefeK_DWxPNkFDvX4xY9Cd_4lq9UkPg130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1022862.RAHkm1WnXAuk2BsefeK_DWxPNkFDvX4xY9Cd_4lq9UkPg130_assertion type Assertion NP1022862.RAHkm1WnXAuk2BsefeK_DWxPNkFDvX4xY9Cd_4lq9UkPg130_head.
- NP1022862.RAHkm1WnXAuk2BsefeK_DWxPNkFDvX4xY9Cd_4lq9UkPg130_assertion description "[A missense mutation from arginine to tryptophan at residue 849 in the kinase domain of Tie2 (Tie2-R849W) is commonly identified in familial venous malformations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1022862.RAHkm1WnXAuk2BsefeK_DWxPNkFDvX4xY9Cd_4lq9UkPg130_provenance.
- NP1022862.RAHkm1WnXAuk2BsefeK_DWxPNkFDvX4xY9Cd_4lq9UkPg130_assertion evidence source_evidence_literature NP1022862.RAHkm1WnXAuk2BsefeK_DWxPNkFDvX4xY9Cd_4lq9UkPg130_provenance.
- NP1022862.RAHkm1WnXAuk2BsefeK_DWxPNkFDvX4xY9Cd_4lq9UkPg130_assertion SIO_000772 23086340 NP1022862.RAHkm1WnXAuk2BsefeK_DWxPNkFDvX4xY9Cd_4lq9UkPg130_provenance.
- NP1022862.RAHkm1WnXAuk2BsefeK_DWxPNkFDvX4xY9Cd_4lq9UkPg130_assertion wasDerivedFrom befree-2016 NP1022862.RAHkm1WnXAuk2BsefeK_DWxPNkFDvX4xY9Cd_4lq9UkPg130_provenance.
- NP1022862.RAHkm1WnXAuk2BsefeK_DWxPNkFDvX4xY9Cd_4lq9UkPg130_assertion wasGeneratedBy ECO_0000203 NP1022862.RAHkm1WnXAuk2BsefeK_DWxPNkFDvX4xY9Cd_4lq9UkPg130_provenance.