Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP874170.RAUsk3oASEU15GbYPdqZ6vYm4iFs2WLdLNCb1ahTiK4fg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP874170.RAUsk3oASEU15GbYPdqZ6vYm4iFs2WLdLNCb1ahTiK4fg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP874170.RAUsk3oASEU15GbYPdqZ6vYm4iFs2WLdLNCb1ahTiK4fg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP874170.RAUsk3oASEU15GbYPdqZ6vYm4iFs2WLdLNCb1ahTiK4fg130_provenance.
- NP874170.RAUsk3oASEU15GbYPdqZ6vYm4iFs2WLdLNCb1ahTiK4fg130_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." NP874170.RAUsk3oASEU15GbYPdqZ6vYm4iFs2WLdLNCb1ahTiK4fg130_provenance.
- NP874170.RAUsk3oASEU15GbYPdqZ6vYm4iFs2WLdLNCb1ahTiK4fg130_assertion evidence source_evidence_literature NP874170.RAUsk3oASEU15GbYPdqZ6vYm4iFs2WLdLNCb1ahTiK4fg130_provenance.
- NP874170.RAUsk3oASEU15GbYPdqZ6vYm4iFs2WLdLNCb1ahTiK4fg130_assertion SIO_000772 21340161 NP874170.RAUsk3oASEU15GbYPdqZ6vYm4iFs2WLdLNCb1ahTiK4fg130_provenance.
- NP874170.RAUsk3oASEU15GbYPdqZ6vYm4iFs2WLdLNCb1ahTiK4fg130_assertion wasDerivedFrom befree-2016 NP874170.RAUsk3oASEU15GbYPdqZ6vYm4iFs2WLdLNCb1ahTiK4fg130_provenance.
- NP874170.RAUsk3oASEU15GbYPdqZ6vYm4iFs2WLdLNCb1ahTiK4fg130_assertion wasGeneratedBy ECO_0000203 NP874170.RAUsk3oASEU15GbYPdqZ6vYm4iFs2WLdLNCb1ahTiK4fg130_provenance.
- befree-2016 importedOn "2016-02-19" NP874170.RAUsk3oASEU15GbYPdqZ6vYm4iFs2WLdLNCb1ahTiK4fg130_provenance.