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- source_evidence_literature type ECO_0000212 NP147357.RAfnVi_pQSdiHqMUzU-tE42ZZb9daSbR6rfGx-y393oMY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP147357.RAfnVi_pQSdiHqMUzU-tE42ZZb9daSbR6rfGx-y393oMY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP147357.RAfnVi_pQSdiHqMUzU-tE42ZZb9daSbR6rfGx-y393oMY130_provenance.
- NP147357.RAfnVi_pQSdiHqMUzU-tE42ZZb9daSbR6rfGx-y393oMY130_assertion wasGeneratedBy ECO_0000203 NP147357.RAfnVi_pQSdiHqMUzU-tE42ZZb9daSbR6rfGx-y393oMY130_provenance.
- NP147357.RAfnVi_pQSdiHqMUzU-tE42ZZb9daSbR6rfGx-y393oMY130_assertion wasDerivedFrom lhgdn-20090331 NP147357.RAfnVi_pQSdiHqMUzU-tE42ZZb9daSbR6rfGx-y393oMY130_provenance.
- NP147357.RAfnVi_pQSdiHqMUzU-tE42ZZb9daSbR6rfGx-y393oMY130_assertion SIO_000772 18429043 NP147357.RAfnVi_pQSdiHqMUzU-tE42ZZb9daSbR6rfGx-y393oMY130_provenance.
- NP147357.RAfnVi_pQSdiHqMUzU-tE42ZZb9daSbR6rfGx-y393oMY130_assertion evidence source_evidence_literature NP147357.RAfnVi_pQSdiHqMUzU-tE42ZZb9daSbR6rfGx-y393oMY130_provenance.
- NP147357.RAfnVi_pQSdiHqMUzU-tE42ZZb9daSbR6rfGx-y393oMY130_assertion description "[Based on our results it is estimated that about 20% of patients with Usher syndrome type I have CDH23 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147357.RAfnVi_pQSdiHqMUzU-tE42ZZb9daSbR6rfGx-y393oMY130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP147357.RAfnVi_pQSdiHqMUzU-tE42ZZb9daSbR6rfGx-y393oMY130_provenance.