Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP894622.RANHTMMhOVxNQNYnnE9GzEP4Zo4mglEFhNAK2wX0LMtOM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP894622.RANHTMMhOVxNQNYnnE9GzEP4Zo4mglEFhNAK2wX0LMtOM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP894622.RANHTMMhOVxNQNYnnE9GzEP4Zo4mglEFhNAK2wX0LMtOM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP894622.RANHTMMhOVxNQNYnnE9GzEP4Zo4mglEFhNAK2wX0LMtOM130_provenance.
- NP894622.RANHTMMhOVxNQNYnnE9GzEP4Zo4mglEFhNAK2wX0LMtOM130_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." NP894622.RANHTMMhOVxNQNYnnE9GzEP4Zo4mglEFhNAK2wX0LMtOM130_provenance.
- NP894622.RANHTMMhOVxNQNYnnE9GzEP4Zo4mglEFhNAK2wX0LMtOM130_assertion evidence source_evidence_literature NP894622.RANHTMMhOVxNQNYnnE9GzEP4Zo4mglEFhNAK2wX0LMtOM130_provenance.
- NP894622.RANHTMMhOVxNQNYnnE9GzEP4Zo4mglEFhNAK2wX0LMtOM130_assertion SIO_000772 20865670 NP894622.RANHTMMhOVxNQNYnnE9GzEP4Zo4mglEFhNAK2wX0LMtOM130_provenance.
- NP894622.RANHTMMhOVxNQNYnnE9GzEP4Zo4mglEFhNAK2wX0LMtOM130_assertion wasDerivedFrom befree-20140225 NP894622.RANHTMMhOVxNQNYnnE9GzEP4Zo4mglEFhNAK2wX0LMtOM130_provenance.
- NP894622.RANHTMMhOVxNQNYnnE9GzEP4Zo4mglEFhNAK2wX0LMtOM130_assertion wasGeneratedBy ECO_0000203 NP894622.RANHTMMhOVxNQNYnnE9GzEP4Zo4mglEFhNAK2wX0LMtOM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP894622.RANHTMMhOVxNQNYnnE9GzEP4Zo4mglEFhNAK2wX0LMtOM130_provenance.