Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP586745.RACodXCAtj6yMgiP7smbNoRYYu3IsSaotKCo0GiRNWTSM130_assertion> ?p ?o ?g. }
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- NP586745.RACodXCAtj6yMgiP7smbNoRYYu3IsSaotKCo0GiRNWTSM130_assertion type Assertion NP586745.RACodXCAtj6yMgiP7smbNoRYYu3IsSaotKCo0GiRNWTSM130_head.
- NP586745.RACodXCAtj6yMgiP7smbNoRYYu3IsSaotKCo0GiRNWTSM130_assertion wasGeneratedBy ECO_0000203 NP586745.RACodXCAtj6yMgiP7smbNoRYYu3IsSaotKCo0GiRNWTSM130_provenance.
- NP586745.RACodXCAtj6yMgiP7smbNoRYYu3IsSaotKCo0GiRNWTSM130_assertion wasDerivedFrom befree-2016 NP586745.RACodXCAtj6yMgiP7smbNoRYYu3IsSaotKCo0GiRNWTSM130_provenance.
- NP586745.RACodXCAtj6yMgiP7smbNoRYYu3IsSaotKCo0GiRNWTSM130_assertion SIO_000772 1719807 NP586745.RACodXCAtj6yMgiP7smbNoRYYu3IsSaotKCo0GiRNWTSM130_provenance.
- NP586745.RACodXCAtj6yMgiP7smbNoRYYu3IsSaotKCo0GiRNWTSM130_assertion evidence source_evidence_literature NP586745.RACodXCAtj6yMgiP7smbNoRYYu3IsSaotKCo0GiRNWTSM130_provenance.
- NP586745.RACodXCAtj6yMgiP7smbNoRYYu3IsSaotKCo0GiRNWTSM130_assertion description "[We report a relatively mild phenotype associated with two siblings who are compound heterozygotes for Hb S and a beta zero-thalassemia mutation due to a approximately 1.4-kb deletion of the 5' region of the beta-globin gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP586745.RACodXCAtj6yMgiP7smbNoRYYu3IsSaotKCo0GiRNWTSM130_provenance.