Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP438613.RAo40TKDdZawU7nzQ0UKmYxRF2u9qj3e93ZpMCAD0EcNg130_assertion> ?p ?o ?g. }
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- NP438613.RAo40TKDdZawU7nzQ0UKmYxRF2u9qj3e93ZpMCAD0EcNg130_assertion type Assertion NP438613.RAo40TKDdZawU7nzQ0UKmYxRF2u9qj3e93ZpMCAD0EcNg130_head.
- NP438613.RAo40TKDdZawU7nzQ0UKmYxRF2u9qj3e93ZpMCAD0EcNg130_assertion wasGeneratedBy ECO_0000203 NP438613.RAo40TKDdZawU7nzQ0UKmYxRF2u9qj3e93ZpMCAD0EcNg130_provenance.
- NP438613.RAo40TKDdZawU7nzQ0UKmYxRF2u9qj3e93ZpMCAD0EcNg130_assertion wasDerivedFrom befree-20140225 NP438613.RAo40TKDdZawU7nzQ0UKmYxRF2u9qj3e93ZpMCAD0EcNg130_provenance.
- NP438613.RAo40TKDdZawU7nzQ0UKmYxRF2u9qj3e93ZpMCAD0EcNg130_assertion SIO_000772 18363760 NP438613.RAo40TKDdZawU7nzQ0UKmYxRF2u9qj3e93ZpMCAD0EcNg130_provenance.
- NP438613.RAo40TKDdZawU7nzQ0UKmYxRF2u9qj3e93ZpMCAD0EcNg130_assertion evidence source_evidence_literature NP438613.RAo40TKDdZawU7nzQ0UKmYxRF2u9qj3e93ZpMCAD0EcNg130_provenance.
- NP438613.RAo40TKDdZawU7nzQ0UKmYxRF2u9qj3e93ZpMCAD0EcNg130_assertion description "[We have demonstrated that the spectrum of clinical manifestations due to mutations in RASA1 is wider than previously thought and also includes typical CMs not associated with AVM/AVF.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP438613.RAo40TKDdZawU7nzQ0UKmYxRF2u9qj3e93ZpMCAD0EcNg130_provenance.