Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP120716.RA_DwTIeo3A23tLXHnEkxquK0hdUhKQhMi7NBY5NIiJiY130_assertion> ?p ?o ?g. }
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- NP120716.RA_DwTIeo3A23tLXHnEkxquK0hdUhKQhMi7NBY5NIiJiY130_assertion type Assertion NP120716.RA_DwTIeo3A23tLXHnEkxquK0hdUhKQhMi7NBY5NIiJiY130_head.
- NP120716.RA_DwTIeo3A23tLXHnEkxquK0hdUhKQhMi7NBY5NIiJiY130_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." NP120716.RA_DwTIeo3A23tLXHnEkxquK0hdUhKQhMi7NBY5NIiJiY130_provenance.
- NP120716.RA_DwTIeo3A23tLXHnEkxquK0hdUhKQhMi7NBY5NIiJiY130_assertion evidence source_evidence_literature NP120716.RA_DwTIeo3A23tLXHnEkxquK0hdUhKQhMi7NBY5NIiJiY130_provenance.
- NP120716.RA_DwTIeo3A23tLXHnEkxquK0hdUhKQhMi7NBY5NIiJiY130_assertion SIO_000772 15952107 NP120716.RA_DwTIeo3A23tLXHnEkxquK0hdUhKQhMi7NBY5NIiJiY130_provenance.
- NP120716.RA_DwTIeo3A23tLXHnEkxquK0hdUhKQhMi7NBY5NIiJiY130_assertion wasDerivedFrom lhgdn-20090331 NP120716.RA_DwTIeo3A23tLXHnEkxquK0hdUhKQhMi7NBY5NIiJiY130_provenance.
- NP120716.RA_DwTIeo3A23tLXHnEkxquK0hdUhKQhMi7NBY5NIiJiY130_assertion wasGeneratedBy ECO_0000203 NP120716.RA_DwTIeo3A23tLXHnEkxquK0hdUhKQhMi7NBY5NIiJiY130_provenance.