Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP420630.RACb94rt3MDRxC7t0zA4yL1YZid0UpBCN6Y8L5MRYTTKo130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP420630.RACb94rt3MDRxC7t0zA4yL1YZid0UpBCN6Y8L5MRYTTKo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP420630.RACb94rt3MDRxC7t0zA4yL1YZid0UpBCN6Y8L5MRYTTKo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP420630.RACb94rt3MDRxC7t0zA4yL1YZid0UpBCN6Y8L5MRYTTKo130_provenance.
- NP420630.RACb94rt3MDRxC7t0zA4yL1YZid0UpBCN6Y8L5MRYTTKo130_assertion description "[Mutant GTP cyclohydrolase I in autosomal dominant dystonia and recessive hyperphenylalaninemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP420630.RACb94rt3MDRxC7t0zA4yL1YZid0UpBCN6Y8L5MRYTTKo130_provenance.
- NP420630.RACb94rt3MDRxC7t0zA4yL1YZid0UpBCN6Y8L5MRYTTKo130_assertion evidence source_evidence_literature NP420630.RACb94rt3MDRxC7t0zA4yL1YZid0UpBCN6Y8L5MRYTTKo130_provenance.
- NP420630.RACb94rt3MDRxC7t0zA4yL1YZid0UpBCN6Y8L5MRYTTKo130_assertion SIO_000772 9921872 NP420630.RACb94rt3MDRxC7t0zA4yL1YZid0UpBCN6Y8L5MRYTTKo130_provenance.
- NP420630.RACb94rt3MDRxC7t0zA4yL1YZid0UpBCN6Y8L5MRYTTKo130_assertion wasDerivedFrom befree-20150227 NP420630.RACb94rt3MDRxC7t0zA4yL1YZid0UpBCN6Y8L5MRYTTKo130_provenance.
- NP420630.RACb94rt3MDRxC7t0zA4yL1YZid0UpBCN6Y8L5MRYTTKo130_assertion wasGeneratedBy ECO_0000203 NP420630.RACb94rt3MDRxC7t0zA4yL1YZid0UpBCN6Y8L5MRYTTKo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP420630.RACb94rt3MDRxC7t0zA4yL1YZid0UpBCN6Y8L5MRYTTKo130_provenance.