Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP697535.RAAFsWkG9u6gbMxCFjdTrRpN8-FhdflsLjWI8jJ7x5wsY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP697535.RAAFsWkG9u6gbMxCFjdTrRpN8-FhdflsLjWI8jJ7x5wsY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP697535.RAAFsWkG9u6gbMxCFjdTrRpN8-FhdflsLjWI8jJ7x5wsY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP697535.RAAFsWkG9u6gbMxCFjdTrRpN8-FhdflsLjWI8jJ7x5wsY130_provenance.
- NP697535.RAAFsWkG9u6gbMxCFjdTrRpN8-FhdflsLjWI8jJ7x5wsY130_assertion description "[Congenital hypothyroidism due to mutations in the sodium/iodide symporter. Identification of a nonsense mutation producing a downstream cryptic 3' splice site.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP697535.RAAFsWkG9u6gbMxCFjdTrRpN8-FhdflsLjWI8jJ7x5wsY130_provenance.
- NP697535.RAAFsWkG9u6gbMxCFjdTrRpN8-FhdflsLjWI8jJ7x5wsY130_assertion evidence source_evidence_literature NP697535.RAAFsWkG9u6gbMxCFjdTrRpN8-FhdflsLjWI8jJ7x5wsY130_provenance.
- NP697535.RAAFsWkG9u6gbMxCFjdTrRpN8-FhdflsLjWI8jJ7x5wsY130_assertion SIO_000772 9486973 NP697535.RAAFsWkG9u6gbMxCFjdTrRpN8-FhdflsLjWI8jJ7x5wsY130_provenance.
- NP697535.RAAFsWkG9u6gbMxCFjdTrRpN8-FhdflsLjWI8jJ7x5wsY130_assertion wasDerivedFrom befree-20150227 NP697535.RAAFsWkG9u6gbMxCFjdTrRpN8-FhdflsLjWI8jJ7x5wsY130_provenance.
- NP697535.RAAFsWkG9u6gbMxCFjdTrRpN8-FhdflsLjWI8jJ7x5wsY130_assertion wasGeneratedBy ECO_0000203 NP697535.RAAFsWkG9u6gbMxCFjdTrRpN8-FhdflsLjWI8jJ7x5wsY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP697535.RAAFsWkG9u6gbMxCFjdTrRpN8-FhdflsLjWI8jJ7x5wsY130_provenance.