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- NP874170.RAUsk3oASEU15GbYPdqZ6vYm4iFs2WLdLNCb1ahTiK4fg130_assertion type Assertion NP874170.RAUsk3oASEU15GbYPdqZ6vYm4iFs2WLdLNCb1ahTiK4fg130_head.
- 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.