Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP784302.RAVcFmjAHuX9hgR5Y2iGR0yrIaFQJ7YnelDYnCt0myXJs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP784302.RAVcFmjAHuX9hgR5Y2iGR0yrIaFQJ7YnelDYnCt0myXJs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP784302.RAVcFmjAHuX9hgR5Y2iGR0yrIaFQJ7YnelDYnCt0myXJs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP784302.RAVcFmjAHuX9hgR5Y2iGR0yrIaFQJ7YnelDYnCt0myXJs130_provenance.
- NP784302.RAVcFmjAHuX9hgR5Y2iGR0yrIaFQJ7YnelDYnCt0myXJs130_assertion description "[Screening for mutations in transcription factors in a Czech cohort of 170 patients with congenital and early-onset hypothyroidism: identification of a novel PAX8 mutation in dominantly inherited early-onset non-autoimmune hypothyroidism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP784302.RAVcFmjAHuX9hgR5Y2iGR0yrIaFQJ7YnelDYnCt0myXJs130_provenance.
- NP784302.RAVcFmjAHuX9hgR5Y2iGR0yrIaFQJ7YnelDYnCt0myXJs130_assertion evidence source_evidence_literature NP784302.RAVcFmjAHuX9hgR5Y2iGR0yrIaFQJ7YnelDYnCt0myXJs130_provenance.
- NP784302.RAVcFmjAHuX9hgR5Y2iGR0yrIaFQJ7YnelDYnCt0myXJs130_assertion SIO_000772 17468187 NP784302.RAVcFmjAHuX9hgR5Y2iGR0yrIaFQJ7YnelDYnCt0myXJs130_provenance.
- NP784302.RAVcFmjAHuX9hgR5Y2iGR0yrIaFQJ7YnelDYnCt0myXJs130_assertion wasDerivedFrom befree-20150227 NP784302.RAVcFmjAHuX9hgR5Y2iGR0yrIaFQJ7YnelDYnCt0myXJs130_provenance.
- NP784302.RAVcFmjAHuX9hgR5Y2iGR0yrIaFQJ7YnelDYnCt0myXJs130_assertion wasGeneratedBy ECO_0000203 NP784302.RAVcFmjAHuX9hgR5Y2iGR0yrIaFQJ7YnelDYnCt0myXJs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP784302.RAVcFmjAHuX9hgR5Y2iGR0yrIaFQJ7YnelDYnCt0myXJs130_provenance.