Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP250350.RAYJvXYR34hva-0IovwAYMDgU5YA_TvHF8kRdeJbYoggk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP250350.RAYJvXYR34hva-0IovwAYMDgU5YA_TvHF8kRdeJbYoggk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP250350.RAYJvXYR34hva-0IovwAYMDgU5YA_TvHF8kRdeJbYoggk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP250350.RAYJvXYR34hva-0IovwAYMDgU5YA_TvHF8kRdeJbYoggk130_provenance.
- NP250350.RAYJvXYR34hva-0IovwAYMDgU5YA_TvHF8kRdeJbYoggk130_assertion description "[Monoallelic thyroid peroxidase gene mutation in a patient with congenital hypothyroidism with total iodide organification defect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP250350.RAYJvXYR34hva-0IovwAYMDgU5YA_TvHF8kRdeJbYoggk130_provenance.
- NP250350.RAYJvXYR34hva-0IovwAYMDgU5YA_TvHF8kRdeJbYoggk130_assertion evidence source_evidence_literature NP250350.RAYJvXYR34hva-0IovwAYMDgU5YA_TvHF8kRdeJbYoggk130_provenance.
- NP250350.RAYJvXYR34hva-0IovwAYMDgU5YA_TvHF8kRdeJbYoggk130_assertion SIO_000772 21340161 NP250350.RAYJvXYR34hva-0IovwAYMDgU5YA_TvHF8kRdeJbYoggk130_provenance.
- NP250350.RAYJvXYR34hva-0IovwAYMDgU5YA_TvHF8kRdeJbYoggk130_assertion wasDerivedFrom befree-20140225 NP250350.RAYJvXYR34hva-0IovwAYMDgU5YA_TvHF8kRdeJbYoggk130_provenance.
- NP250350.RAYJvXYR34hva-0IovwAYMDgU5YA_TvHF8kRdeJbYoggk130_assertion wasGeneratedBy ECO_0000203 NP250350.RAYJvXYR34hva-0IovwAYMDgU5YA_TvHF8kRdeJbYoggk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP250350.RAYJvXYR34hva-0IovwAYMDgU5YA_TvHF8kRdeJbYoggk130_provenance.