Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP862887.RAwtVvuE3HyLaDVUw7mpYTh-VRQ2cMmaCbUjFltbgEsnQ130_assertion> ?p ?o ?g. }
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- NP862887.RAwtVvuE3HyLaDVUw7mpYTh-VRQ2cMmaCbUjFltbgEsnQ130_assertion type Assertion NP862887.RAwtVvuE3HyLaDVUw7mpYTh-VRQ2cMmaCbUjFltbgEsnQ130_head.
- NP862887.RAwtVvuE3HyLaDVUw7mpYTh-VRQ2cMmaCbUjFltbgEsnQ130_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." NP862887.RAwtVvuE3HyLaDVUw7mpYTh-VRQ2cMmaCbUjFltbgEsnQ130_provenance.
- NP862887.RAwtVvuE3HyLaDVUw7mpYTh-VRQ2cMmaCbUjFltbgEsnQ130_assertion evidence source_evidence_literature NP862887.RAwtVvuE3HyLaDVUw7mpYTh-VRQ2cMmaCbUjFltbgEsnQ130_provenance.
- NP862887.RAwtVvuE3HyLaDVUw7mpYTh-VRQ2cMmaCbUjFltbgEsnQ130_assertion SIO_000772 20865670 NP862887.RAwtVvuE3HyLaDVUw7mpYTh-VRQ2cMmaCbUjFltbgEsnQ130_provenance.
- NP862887.RAwtVvuE3HyLaDVUw7mpYTh-VRQ2cMmaCbUjFltbgEsnQ130_assertion wasDerivedFrom befree-20140225 NP862887.RAwtVvuE3HyLaDVUw7mpYTh-VRQ2cMmaCbUjFltbgEsnQ130_provenance.
- NP862887.RAwtVvuE3HyLaDVUw7mpYTh-VRQ2cMmaCbUjFltbgEsnQ130_assertion wasGeneratedBy ECO_0000203 NP862887.RAwtVvuE3HyLaDVUw7mpYTh-VRQ2cMmaCbUjFltbgEsnQ130_provenance.