Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP198633.RAg2NLUsHEdCLWjxfHPu39on6Q2jMwaiKzHhgzQrgeWAE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP198633.RAg2NLUsHEdCLWjxfHPu39on6Q2jMwaiKzHhgzQrgeWAE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP198633.RAg2NLUsHEdCLWjxfHPu39on6Q2jMwaiKzHhgzQrgeWAE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP198633.RAg2NLUsHEdCLWjxfHPu39on6Q2jMwaiKzHhgzQrgeWAE130_provenance.
- NP198633.RAg2NLUsHEdCLWjxfHPu39on6Q2jMwaiKzHhgzQrgeWAE130_assertion description "[Two novel missense mutations in the thyroid peroxidase gene, R665W and G771R, result in a localization defect and cause congenital hypothyroidism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP198633.RAg2NLUsHEdCLWjxfHPu39on6Q2jMwaiKzHhgzQrgeWAE130_provenance.
- NP198633.RAg2NLUsHEdCLWjxfHPu39on6Q2jMwaiKzHhgzQrgeWAE130_assertion evidence source_evidence_literature NP198633.RAg2NLUsHEdCLWjxfHPu39on6Q2jMwaiKzHhgzQrgeWAE130_provenance.
- NP198633.RAg2NLUsHEdCLWjxfHPu39on6Q2jMwaiKzHhgzQrgeWAE130_assertion SIO_000772 11916616 NP198633.RAg2NLUsHEdCLWjxfHPu39on6Q2jMwaiKzHhgzQrgeWAE130_provenance.
- NP198633.RAg2NLUsHEdCLWjxfHPu39on6Q2jMwaiKzHhgzQrgeWAE130_assertion wasDerivedFrom lhgdn-20090331 NP198633.RAg2NLUsHEdCLWjxfHPu39on6Q2jMwaiKzHhgzQrgeWAE130_provenance.
- NP198633.RAg2NLUsHEdCLWjxfHPu39on6Q2jMwaiKzHhgzQrgeWAE130_assertion wasGeneratedBy ECO_0000203 NP198633.RAg2NLUsHEdCLWjxfHPu39on6Q2jMwaiKzHhgzQrgeWAE130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP198633.RAg2NLUsHEdCLWjxfHPu39on6Q2jMwaiKzHhgzQrgeWAE130_provenance.