Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP232550.RALjpErpy4-Se059BzH2Tsk9Xn7rsQL1wVhZgAEHDMuYc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP232550.RALjpErpy4-Se059BzH2Tsk9Xn7rsQL1wVhZgAEHDMuYc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP232550.RALjpErpy4-Se059BzH2Tsk9Xn7rsQL1wVhZgAEHDMuYc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP232550.RALjpErpy4-Se059BzH2Tsk9Xn7rsQL1wVhZgAEHDMuYc130_provenance.
- NP232550.RALjpErpy4-Se059BzH2Tsk9Xn7rsQL1wVhZgAEHDMuYc130_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." NP232550.RALjpErpy4-Se059BzH2Tsk9Xn7rsQL1wVhZgAEHDMuYc130_provenance.
- NP232550.RALjpErpy4-Se059BzH2Tsk9Xn7rsQL1wVhZgAEHDMuYc130_assertion evidence source_evidence_literature NP232550.RALjpErpy4-Se059BzH2Tsk9Xn7rsQL1wVhZgAEHDMuYc130_provenance.
- NP232550.RALjpErpy4-Se059BzH2Tsk9Xn7rsQL1wVhZgAEHDMuYc130_assertion SIO_000772 9921872 NP232550.RALjpErpy4-Se059BzH2Tsk9Xn7rsQL1wVhZgAEHDMuYc130_provenance.
- NP232550.RALjpErpy4-Se059BzH2Tsk9Xn7rsQL1wVhZgAEHDMuYc130_assertion wasDerivedFrom befree-20140225 NP232550.RALjpErpy4-Se059BzH2Tsk9Xn7rsQL1wVhZgAEHDMuYc130_provenance.
- NP232550.RALjpErpy4-Se059BzH2Tsk9Xn7rsQL1wVhZgAEHDMuYc130_assertion wasGeneratedBy ECO_0000203 NP232550.RALjpErpy4-Se059BzH2Tsk9Xn7rsQL1wVhZgAEHDMuYc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP232550.RALjpErpy4-Se059BzH2Tsk9Xn7rsQL1wVhZgAEHDMuYc130_provenance.