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- NP841626.RAUG_jmnY1JTmFdnuM26PkThdQK-qPLFfl9OpJAXtyfc4130_assertion type Assertion NP841626.RAUG_jmnY1JTmFdnuM26PkThdQK-qPLFfl9OpJAXtyfc4130_head.
- NP841626.RAUG_jmnY1JTmFdnuM26PkThdQK-qPLFfl9OpJAXtyfc4130_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." NP841626.RAUG_jmnY1JTmFdnuM26PkThdQK-qPLFfl9OpJAXtyfc4130_provenance.
- NP841626.RAUG_jmnY1JTmFdnuM26PkThdQK-qPLFfl9OpJAXtyfc4130_assertion evidence source_evidence_literature NP841626.RAUG_jmnY1JTmFdnuM26PkThdQK-qPLFfl9OpJAXtyfc4130_provenance.
- NP841626.RAUG_jmnY1JTmFdnuM26PkThdQK-qPLFfl9OpJAXtyfc4130_assertion SIO_000772 20865670 NP841626.RAUG_jmnY1JTmFdnuM26PkThdQK-qPLFfl9OpJAXtyfc4130_provenance.
- NP841626.RAUG_jmnY1JTmFdnuM26PkThdQK-qPLFfl9OpJAXtyfc4130_assertion wasDerivedFrom befree-2016 NP841626.RAUG_jmnY1JTmFdnuM26PkThdQK-qPLFfl9OpJAXtyfc4130_provenance.
- NP841626.RAUG_jmnY1JTmFdnuM26PkThdQK-qPLFfl9OpJAXtyfc4130_assertion wasGeneratedBy ECO_0000203 NP841626.RAUG_jmnY1JTmFdnuM26PkThdQK-qPLFfl9OpJAXtyfc4130_provenance.