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- source_evidence_literature type ECO_0000212 NP209178.RA7zbc7h-o-hFSsWHEogIQ7mgBtm9Dxo74dZSBAS69Ja8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP209178.RA7zbc7h-o-hFSsWHEogIQ7mgBtm9Dxo74dZSBAS69Ja8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP209178.RA7zbc7h-o-hFSsWHEogIQ7mgBtm9Dxo74dZSBAS69Ja8130_provenance.
- NP209178.RA7zbc7h-o-hFSsWHEogIQ7mgBtm9Dxo74dZSBAS69Ja8130_assertion description "[Biallelic mutations in the NIS gene lead to a congenital iodide transport defect, an autosomal recessive condition characterized by hypothyroidism, goiter, low thyroid iodide uptake, and a low saliva/plasma iodide ratio.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP209178.RA7zbc7h-o-hFSsWHEogIQ7mgBtm9Dxo74dZSBAS69Ja8130_provenance.
- NP209178.RA7zbc7h-o-hFSsWHEogIQ7mgBtm9Dxo74dZSBAS69Ja8130_assertion evidence source_evidence_literature NP209178.RA7zbc7h-o-hFSsWHEogIQ7mgBtm9Dxo74dZSBAS69Ja8130_provenance.
- NP209178.RA7zbc7h-o-hFSsWHEogIQ7mgBtm9Dxo74dZSBAS69Ja8130_assertion SIO_000772 19196800 NP209178.RA7zbc7h-o-hFSsWHEogIQ7mgBtm9Dxo74dZSBAS69Ja8130_provenance.
- NP209178.RA7zbc7h-o-hFSsWHEogIQ7mgBtm9Dxo74dZSBAS69Ja8130_assertion wasDerivedFrom lhgdn-20090331 NP209178.RA7zbc7h-o-hFSsWHEogIQ7mgBtm9Dxo74dZSBAS69Ja8130_provenance.
- NP209178.RA7zbc7h-o-hFSsWHEogIQ7mgBtm9Dxo74dZSBAS69Ja8130_assertion wasGeneratedBy ECO_0000203 NP209178.RA7zbc7h-o-hFSsWHEogIQ7mgBtm9Dxo74dZSBAS69Ja8130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP209178.RA7zbc7h-o-hFSsWHEogIQ7mgBtm9Dxo74dZSBAS69Ja8130_provenance.