Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP978057.RA0YCqGAehSKHWkTivuuB_3pydUbJ6ABASvRDcfi_Ko8g130_assertion> ?p ?o ?g. }
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- NP978057.RA0YCqGAehSKHWkTivuuB_3pydUbJ6ABASvRDcfi_Ko8g130_assertion type Assertion NP978057.RA0YCqGAehSKHWkTivuuB_3pydUbJ6ABASvRDcfi_Ko8g130_head.
- NP978057.RA0YCqGAehSKHWkTivuuB_3pydUbJ6ABASvRDcfi_Ko8g130_assertion description "[Mutations in human GLIS3 have been implicated in a syndrome characterized by neonatal diabetes and congenital hypothyroidism (NDH) and in some patients accompanied by polycystic kidney disease, glaucoma, and liver fibrosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978057.RA0YCqGAehSKHWkTivuuB_3pydUbJ6ABASvRDcfi_Ko8g130_provenance.
- NP978057.RA0YCqGAehSKHWkTivuuB_3pydUbJ6ABASvRDcfi_Ko8g130_assertion evidence source_evidence_literature NP978057.RA0YCqGAehSKHWkTivuuB_3pydUbJ6ABASvRDcfi_Ko8g130_provenance.
- NP978057.RA0YCqGAehSKHWkTivuuB_3pydUbJ6ABASvRDcfi_Ko8g130_assertion SIO_000772 20865670 NP978057.RA0YCqGAehSKHWkTivuuB_3pydUbJ6ABASvRDcfi_Ko8g130_provenance.
- NP978057.RA0YCqGAehSKHWkTivuuB_3pydUbJ6ABASvRDcfi_Ko8g130_assertion wasDerivedFrom befree-20150227 NP978057.RA0YCqGAehSKHWkTivuuB_3pydUbJ6ABASvRDcfi_Ko8g130_provenance.
- NP978057.RA0YCqGAehSKHWkTivuuB_3pydUbJ6ABASvRDcfi_Ko8g130_assertion wasGeneratedBy ECO_0000203 NP978057.RA0YCqGAehSKHWkTivuuB_3pydUbJ6ABASvRDcfi_Ko8g130_provenance.