Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1022862.RAHkm1WnXAuk2BsefeK_DWxPNkFDvX4xY9Cd_4lq9UkPg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1022862.RAHkm1WnXAuk2BsefeK_DWxPNkFDvX4xY9Cd_4lq9UkPg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1022862.RAHkm1WnXAuk2BsefeK_DWxPNkFDvX4xY9Cd_4lq9UkPg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1022862.RAHkm1WnXAuk2BsefeK_DWxPNkFDvX4xY9Cd_4lq9UkPg130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP1022862.RAHkm1WnXAuk2BsefeK_DWxPNkFDvX4xY9Cd_4lq9UkPg130_provenance.