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- NP588241.RAHnefOuA8XEIY_liAV0JHFwaDsxe4jZpOX7ynV-gGzq0130_assertion type Assertion NP588241.RAHnefOuA8XEIY_liAV0JHFwaDsxe4jZpOX7ynV-gGzq0130_head.
- NP588241.RAHnefOuA8XEIY_liAV0JHFwaDsxe4jZpOX7ynV-gGzq0130_assertion wasGeneratedBy ECO_0000203 NP588241.RAHnefOuA8XEIY_liAV0JHFwaDsxe4jZpOX7ynV-gGzq0130_provenance.
- NP588241.RAHnefOuA8XEIY_liAV0JHFwaDsxe4jZpOX7ynV-gGzq0130_assertion wasDerivedFrom befree-2016 NP588241.RAHnefOuA8XEIY_liAV0JHFwaDsxe4jZpOX7ynV-gGzq0130_provenance.
- NP588241.RAHnefOuA8XEIY_liAV0JHFwaDsxe4jZpOX7ynV-gGzq0130_assertion SIO_000772 17216245 NP588241.RAHnefOuA8XEIY_liAV0JHFwaDsxe4jZpOX7ynV-gGzq0130_provenance.
- NP588241.RAHnefOuA8XEIY_liAV0JHFwaDsxe4jZpOX7ynV-gGzq0130_assertion evidence source_evidence_literature NP588241.RAHnefOuA8XEIY_liAV0JHFwaDsxe4jZpOX7ynV-gGzq0130_provenance.
- NP588241.RAHnefOuA8XEIY_liAV0JHFwaDsxe4jZpOX7ynV-gGzq0130_assertion description "[Lack of NPHP2 mutations in a newborn infant with Joubert syndrome-related disorder presenting as end-stage renal disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP588241.RAHnefOuA8XEIY_liAV0JHFwaDsxe4jZpOX7ynV-gGzq0130_provenance.