Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP839522.RAsTvuezqK6-RLfVMk7jKQkfp6hjQUYaSLrElGK1QwOjU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP839522.RAsTvuezqK6-RLfVMk7jKQkfp6hjQUYaSLrElGK1QwOjU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP839522.RAsTvuezqK6-RLfVMk7jKQkfp6hjQUYaSLrElGK1QwOjU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP839522.RAsTvuezqK6-RLfVMk7jKQkfp6hjQUYaSLrElGK1QwOjU130_provenance.
- NP839522.RAsTvuezqK6-RLfVMk7jKQkfp6hjQUYaSLrElGK1QwOjU130_assertion description "[Asymmetric phenotype of Axenfeld-Rieger anomaly and aniridia associated with a novel PITX2 mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP839522.RAsTvuezqK6-RLfVMk7jKQkfp6hjQUYaSLrElGK1QwOjU130_provenance.
- NP839522.RAsTvuezqK6-RLfVMk7jKQkfp6hjQUYaSLrElGK1QwOjU130_assertion evidence source_evidence_literature NP839522.RAsTvuezqK6-RLfVMk7jKQkfp6hjQUYaSLrElGK1QwOjU130_provenance.
- NP839522.RAsTvuezqK6-RLfVMk7jKQkfp6hjQUYaSLrElGK1QwOjU130_assertion SIO_000772 21617748 NP839522.RAsTvuezqK6-RLfVMk7jKQkfp6hjQUYaSLrElGK1QwOjU130_provenance.
- NP839522.RAsTvuezqK6-RLfVMk7jKQkfp6hjQUYaSLrElGK1QwOjU130_assertion wasDerivedFrom befree-20140225 NP839522.RAsTvuezqK6-RLfVMk7jKQkfp6hjQUYaSLrElGK1QwOjU130_provenance.
- NP839522.RAsTvuezqK6-RLfVMk7jKQkfp6hjQUYaSLrElGK1QwOjU130_assertion wasGeneratedBy ECO_0000203 NP839522.RAsTvuezqK6-RLfVMk7jKQkfp6hjQUYaSLrElGK1QwOjU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP839522.RAsTvuezqK6-RLfVMk7jKQkfp6hjQUYaSLrElGK1QwOjU130_provenance.