Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP723207.RAvL3HWcdoKJjA3OpiFKhBmc9xYunyGJBMQa1pGFygPT8130_assertion> ?p ?o ?g. }
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- NP723207.RAvL3HWcdoKJjA3OpiFKhBmc9xYunyGJBMQa1pGFygPT8130_assertion type Assertion NP723207.RAvL3HWcdoKJjA3OpiFKhBmc9xYunyGJBMQa1pGFygPT8130_head.
- NP723207.RAvL3HWcdoKJjA3OpiFKhBmc9xYunyGJBMQa1pGFygPT8130_assertion description "[Mutations in JAG1 were detected in three patients with Alagille syndrome (1.3%), while NKX2.5 mutations were seen in two patients with non-syndromic ToF (0.9%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP723207.RAvL3HWcdoKJjA3OpiFKhBmc9xYunyGJBMQa1pGFygPT8130_provenance.
- NP723207.RAvL3HWcdoKJjA3OpiFKhBmc9xYunyGJBMQa1pGFygPT8130_assertion evidence source_evidence_literature NP723207.RAvL3HWcdoKJjA3OpiFKhBmc9xYunyGJBMQa1pGFygPT8130_provenance.
- NP723207.RAvL3HWcdoKJjA3OpiFKhBmc9xYunyGJBMQa1pGFygPT8130_assertion SIO_000772 19948535 NP723207.RAvL3HWcdoKJjA3OpiFKhBmc9xYunyGJBMQa1pGFygPT8130_provenance.
- NP723207.RAvL3HWcdoKJjA3OpiFKhBmc9xYunyGJBMQa1pGFygPT8130_assertion wasDerivedFrom befree-20140225 NP723207.RAvL3HWcdoKJjA3OpiFKhBmc9xYunyGJBMQa1pGFygPT8130_provenance.
- NP723207.RAvL3HWcdoKJjA3OpiFKhBmc9xYunyGJBMQa1pGFygPT8130_assertion wasGeneratedBy ECO_0000203 NP723207.RAvL3HWcdoKJjA3OpiFKhBmc9xYunyGJBMQa1pGFygPT8130_provenance.