Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP183908.RArjNS-YIA2_m3N9VNS8fVzFEIwsZHTl5jiTsDlivg-Js130_assertion> ?p ?o ?g. }
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- NP183908.RArjNS-YIA2_m3N9VNS8fVzFEIwsZHTl5jiTsDlivg-Js130_assertion type Assertion NP183908.RArjNS-YIA2_m3N9VNS8fVzFEIwsZHTl5jiTsDlivg-Js130_head.
- NP183908.RArjNS-YIA2_m3N9VNS8fVzFEIwsZHTl5jiTsDlivg-Js130_assertion description "[Data show that mutation of acceptor splice site of the SEDL gene in X-linked spondyloepiphyseal dysplasia tarda causes the activation of cryptic splice site.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP183908.RArjNS-YIA2_m3N9VNS8fVzFEIwsZHTl5jiTsDlivg-Js130_provenance.
- NP183908.RArjNS-YIA2_m3N9VNS8fVzFEIwsZHTl5jiTsDlivg-Js130_assertion evidence source_evidence_literature NP183908.RArjNS-YIA2_m3N9VNS8fVzFEIwsZHTl5jiTsDlivg-Js130_provenance.
- NP183908.RArjNS-YIA2_m3N9VNS8fVzFEIwsZHTl5jiTsDlivg-Js130_assertion SIO_000772 15952107 NP183908.RArjNS-YIA2_m3N9VNS8fVzFEIwsZHTl5jiTsDlivg-Js130_provenance.
- NP183908.RArjNS-YIA2_m3N9VNS8fVzFEIwsZHTl5jiTsDlivg-Js130_assertion wasDerivedFrom lhgdn-20090331 NP183908.RArjNS-YIA2_m3N9VNS8fVzFEIwsZHTl5jiTsDlivg-Js130_provenance.
- NP183908.RArjNS-YIA2_m3N9VNS8fVzFEIwsZHTl5jiTsDlivg-Js130_assertion wasGeneratedBy ECO_0000203 NP183908.RArjNS-YIA2_m3N9VNS8fVzFEIwsZHTl5jiTsDlivg-Js130_provenance.