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- source_evidence_literature type ECO_0000212 NP269268.RAYXEfmAd0wxx_Rl45hbYOzyyZQ5_TH1R_WNUNqyKA9cA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP269268.RAYXEfmAd0wxx_Rl45hbYOzyyZQ5_TH1R_WNUNqyKA9cA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP269268.RAYXEfmAd0wxx_Rl45hbYOzyyZQ5_TH1R_WNUNqyKA9cA130_provenance.
- NP269268.RAYXEfmAd0wxx_Rl45hbYOzyyZQ5_TH1R_WNUNqyKA9cA130_assertion description "[To further characterize the role of NKX2.5 in cardiac morphogenesis, we sought additional mutations in groups of probands with cardiac anomalies and first-degree AV block, idiopathic AV block, or tetralogy of Fallot.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP269268.RAYXEfmAd0wxx_Rl45hbYOzyyZQ5_TH1R_WNUNqyKA9cA130_provenance.
- NP269268.RAYXEfmAd0wxx_Rl45hbYOzyyZQ5_TH1R_WNUNqyKA9cA130_assertion evidence source_evidence_literature NP269268.RAYXEfmAd0wxx_Rl45hbYOzyyZQ5_TH1R_WNUNqyKA9cA130_provenance.
- NP269268.RAYXEfmAd0wxx_Rl45hbYOzyyZQ5_TH1R_WNUNqyKA9cA130_assertion SIO_000772 10587520 NP269268.RAYXEfmAd0wxx_Rl45hbYOzyyZQ5_TH1R_WNUNqyKA9cA130_provenance.
- NP269268.RAYXEfmAd0wxx_Rl45hbYOzyyZQ5_TH1R_WNUNqyKA9cA130_assertion wasDerivedFrom befree-2016 NP269268.RAYXEfmAd0wxx_Rl45hbYOzyyZQ5_TH1R_WNUNqyKA9cA130_provenance.
- NP269268.RAYXEfmAd0wxx_Rl45hbYOzyyZQ5_TH1R_WNUNqyKA9cA130_assertion wasGeneratedBy ECO_0000203 NP269268.RAYXEfmAd0wxx_Rl45hbYOzyyZQ5_TH1R_WNUNqyKA9cA130_provenance.
- befree-2016 importedOn "2016-02-19" NP269268.RAYXEfmAd0wxx_Rl45hbYOzyyZQ5_TH1R_WNUNqyKA9cA130_provenance.