Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP935648.RAXyb0VnYwHeVv-Hd7-GV9YghQivUsV8KH7IQxNyKOh-w130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP935648.RAXyb0VnYwHeVv-Hd7-GV9YghQivUsV8KH7IQxNyKOh-w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP935648.RAXyb0VnYwHeVv-Hd7-GV9YghQivUsV8KH7IQxNyKOh-w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP935648.RAXyb0VnYwHeVv-Hd7-GV9YghQivUsV8KH7IQxNyKOh-w130_provenance.
- NP935648.RAXyb0VnYwHeVv-Hd7-GV9YghQivUsV8KH7IQxNyKOh-w130_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." NP935648.RAXyb0VnYwHeVv-Hd7-GV9YghQivUsV8KH7IQxNyKOh-w130_provenance.
- NP935648.RAXyb0VnYwHeVv-Hd7-GV9YghQivUsV8KH7IQxNyKOh-w130_assertion evidence source_evidence_literature NP935648.RAXyb0VnYwHeVv-Hd7-GV9YghQivUsV8KH7IQxNyKOh-w130_provenance.
- NP935648.RAXyb0VnYwHeVv-Hd7-GV9YghQivUsV8KH7IQxNyKOh-w130_assertion SIO_000772 9921872 NP935648.RAXyb0VnYwHeVv-Hd7-GV9YghQivUsV8KH7IQxNyKOh-w130_provenance.
- NP935648.RAXyb0VnYwHeVv-Hd7-GV9YghQivUsV8KH7IQxNyKOh-w130_assertion wasDerivedFrom befree-20150227 NP935648.RAXyb0VnYwHeVv-Hd7-GV9YghQivUsV8KH7IQxNyKOh-w130_provenance.
- NP935648.RAXyb0VnYwHeVv-Hd7-GV9YghQivUsV8KH7IQxNyKOh-w130_assertion wasGeneratedBy ECO_0000203 NP935648.RAXyb0VnYwHeVv-Hd7-GV9YghQivUsV8KH7IQxNyKOh-w130_provenance.
- befree-20150227 importedOn "2015-02-27" NP935648.RAXyb0VnYwHeVv-Hd7-GV9YghQivUsV8KH7IQxNyKOh-w130_provenance.