Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1413613.RA0sWfB08iPaZvG7afpbAP6ZAZvDqyGXT2K6kj_sWyP2A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1413613.RA0sWfB08iPaZvG7afpbAP6ZAZvDqyGXT2K6kj_sWyP2A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1413613.RA0sWfB08iPaZvG7afpbAP6ZAZvDqyGXT2K6kj_sWyP2A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1413613.RA0sWfB08iPaZvG7afpbAP6ZAZvDqyGXT2K6kj_sWyP2A130_provenance.
- NP1413613.RA0sWfB08iPaZvG7afpbAP6ZAZvDqyGXT2K6kj_sWyP2A130_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." NP1413613.RA0sWfB08iPaZvG7afpbAP6ZAZvDqyGXT2K6kj_sWyP2A130_provenance.
- NP1413613.RA0sWfB08iPaZvG7afpbAP6ZAZvDqyGXT2K6kj_sWyP2A130_assertion evidence source_evidence_literature NP1413613.RA0sWfB08iPaZvG7afpbAP6ZAZvDqyGXT2K6kj_sWyP2A130_provenance.
- NP1413613.RA0sWfB08iPaZvG7afpbAP6ZAZvDqyGXT2K6kj_sWyP2A130_assertion SIO_000772 9921872 NP1413613.RA0sWfB08iPaZvG7afpbAP6ZAZvDqyGXT2K6kj_sWyP2A130_provenance.
- NP1413613.RA0sWfB08iPaZvG7afpbAP6ZAZvDqyGXT2K6kj_sWyP2A130_assertion wasDerivedFrom befree-2016 NP1413613.RA0sWfB08iPaZvG7afpbAP6ZAZvDqyGXT2K6kj_sWyP2A130_provenance.
- NP1413613.RA0sWfB08iPaZvG7afpbAP6ZAZvDqyGXT2K6kj_sWyP2A130_assertion wasGeneratedBy ECO_0000203 NP1413613.RA0sWfB08iPaZvG7afpbAP6ZAZvDqyGXT2K6kj_sWyP2A130_provenance.
- befree-2016 importedOn "2016-02-19" NP1413613.RA0sWfB08iPaZvG7afpbAP6ZAZvDqyGXT2K6kj_sWyP2A130_provenance.