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- NP874169.RAmi_HKxB6cLJppq5I_f7prDJ3BmhcDVoA91Pph6F9FI8130_assertion type Assertion NP874169.RAmi_HKxB6cLJppq5I_f7prDJ3BmhcDVoA91Pph6F9FI8130_head.
- NP874169.RAmi_HKxB6cLJppq5I_f7prDJ3BmhcDVoA91Pph6F9FI8130_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." NP874169.RAmi_HKxB6cLJppq5I_f7prDJ3BmhcDVoA91Pph6F9FI8130_provenance.
- NP874169.RAmi_HKxB6cLJppq5I_f7prDJ3BmhcDVoA91Pph6F9FI8130_assertion evidence source_evidence_literature NP874169.RAmi_HKxB6cLJppq5I_f7prDJ3BmhcDVoA91Pph6F9FI8130_provenance.
- NP874169.RAmi_HKxB6cLJppq5I_f7prDJ3BmhcDVoA91Pph6F9FI8130_assertion SIO_000772 21340161 NP874169.RAmi_HKxB6cLJppq5I_f7prDJ3BmhcDVoA91Pph6F9FI8130_provenance.
- NP874169.RAmi_HKxB6cLJppq5I_f7prDJ3BmhcDVoA91Pph6F9FI8130_assertion wasDerivedFrom befree-2016 NP874169.RAmi_HKxB6cLJppq5I_f7prDJ3BmhcDVoA91Pph6F9FI8130_provenance.
- NP874169.RAmi_HKxB6cLJppq5I_f7prDJ3BmhcDVoA91Pph6F9FI8130_assertion wasGeneratedBy ECO_0000203 NP874169.RAmi_HKxB6cLJppq5I_f7prDJ3BmhcDVoA91Pph6F9FI8130_provenance.