Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP756883.RA8Xs081algKMPtDq0GPtSm7nZwfC_ZBRxDFHI9XlXXcA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP756883.RA8Xs081algKMPtDq0GPtSm7nZwfC_ZBRxDFHI9XlXXcA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP756883.RA8Xs081algKMPtDq0GPtSm7nZwfC_ZBRxDFHI9XlXXcA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP756883.RA8Xs081algKMPtDq0GPtSm7nZwfC_ZBRxDFHI9XlXXcA130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP756883.RA8Xs081algKMPtDq0GPtSm7nZwfC_ZBRxDFHI9XlXXcA130_provenance.