Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP902464.RALMFvaWjNmY931f1HA6MkI1nFoN1Lh5zS7O0xbD_LGSw130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP902464.RALMFvaWjNmY931f1HA6MkI1nFoN1Lh5zS7O0xbD_LGSw130_assertion type Assertion NP902464.RALMFvaWjNmY931f1HA6MkI1nFoN1Lh5zS7O0xbD_LGSw130_head.
- NP902464.RALMFvaWjNmY931f1HA6MkI1nFoN1Lh5zS7O0xbD_LGSw130_assertion description "[Expression of sumoylation deficient Nkx2.5 mutant in Nkx2.5 haploinsufficient mice leads to congenital heart defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP902464.RALMFvaWjNmY931f1HA6MkI1nFoN1Lh5zS7O0xbD_LGSw130_provenance.
- NP902464.RALMFvaWjNmY931f1HA6MkI1nFoN1Lh5zS7O0xbD_LGSw130_assertion evidence source_evidence_literature NP902464.RALMFvaWjNmY931f1HA6MkI1nFoN1Lh5zS7O0xbD_LGSw130_provenance.
- NP902464.RALMFvaWjNmY931f1HA6MkI1nFoN1Lh5zS7O0xbD_LGSw130_assertion SIO_000772 21677783 NP902464.RALMFvaWjNmY931f1HA6MkI1nFoN1Lh5zS7O0xbD_LGSw130_provenance.
- NP902464.RALMFvaWjNmY931f1HA6MkI1nFoN1Lh5zS7O0xbD_LGSw130_assertion wasDerivedFrom befree-2016 NP902464.RALMFvaWjNmY931f1HA6MkI1nFoN1Lh5zS7O0xbD_LGSw130_provenance.
- NP902464.RALMFvaWjNmY931f1HA6MkI1nFoN1Lh5zS7O0xbD_LGSw130_assertion wasGeneratedBy ECO_0000203 NP902464.RALMFvaWjNmY931f1HA6MkI1nFoN1Lh5zS7O0xbD_LGSw130_provenance.