Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP756883.RA8Xs081algKMPtDq0GPtSm7nZwfC_ZBRxDFHI9XlXXcA130_assertion> ?p ?o ?g. }
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- NP756883.RA8Xs081algKMPtDq0GPtSm7nZwfC_ZBRxDFHI9XlXXcA130_assertion type Assertion NP756883.RA8Xs081algKMPtDq0GPtSm7nZwfC_ZBRxDFHI9XlXXcA130_head.
- NP756883.RA8Xs081algKMPtDq0GPtSm7nZwfC_ZBRxDFHI9XlXXcA130_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." NP756883.RA8Xs081algKMPtDq0GPtSm7nZwfC_ZBRxDFHI9XlXXcA130_provenance.
- NP756883.RA8Xs081algKMPtDq0GPtSm7nZwfC_ZBRxDFHI9XlXXcA130_assertion evidence source_evidence_literature NP756883.RA8Xs081algKMPtDq0GPtSm7nZwfC_ZBRxDFHI9XlXXcA130_provenance.
- NP756883.RA8Xs081algKMPtDq0GPtSm7nZwfC_ZBRxDFHI9XlXXcA130_assertion SIO_000772 21340161 NP756883.RA8Xs081algKMPtDq0GPtSm7nZwfC_ZBRxDFHI9XlXXcA130_provenance.
- NP756883.RA8Xs081algKMPtDq0GPtSm7nZwfC_ZBRxDFHI9XlXXcA130_assertion wasDerivedFrom befree-20150227 NP756883.RA8Xs081algKMPtDq0GPtSm7nZwfC_ZBRxDFHI9XlXXcA130_provenance.
- NP756883.RA8Xs081algKMPtDq0GPtSm7nZwfC_ZBRxDFHI9XlXXcA130_assertion wasGeneratedBy ECO_0000203 NP756883.RA8Xs081algKMPtDq0GPtSm7nZwfC_ZBRxDFHI9XlXXcA130_provenance.