Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP418763.RAHWGkXpdctBqftgKzqRDvlQqPUCTcn5Rjovi6bvkyJcg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP418763.RAHWGkXpdctBqftgKzqRDvlQqPUCTcn5Rjovi6bvkyJcg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP418763.RAHWGkXpdctBqftgKzqRDvlQqPUCTcn5Rjovi6bvkyJcg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP418763.RAHWGkXpdctBqftgKzqRDvlQqPUCTcn5Rjovi6bvkyJcg130_provenance.
- NP418763.RAHWGkXpdctBqftgKzqRDvlQqPUCTcn5Rjovi6bvkyJcg130_assertion description "[Group 2 comprised 23 patients homozygous for mutations within SLC3A1, that is genetic findings in accordance with the excretion pattern of classic type I cystinuria.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP418763.RAHWGkXpdctBqftgKzqRDvlQqPUCTcn5Rjovi6bvkyJcg130_provenance.
- NP418763.RAHWGkXpdctBqftgKzqRDvlQqPUCTcn5Rjovi6bvkyJcg130_assertion evidence source_evidence_literature NP418763.RAHWGkXpdctBqftgKzqRDvlQqPUCTcn5Rjovi6bvkyJcg130_provenance.
- NP418763.RAHWGkXpdctBqftgKzqRDvlQqPUCTcn5Rjovi6bvkyJcg130_assertion SIO_000772 14586528 NP418763.RAHWGkXpdctBqftgKzqRDvlQqPUCTcn5Rjovi6bvkyJcg130_provenance.
- NP418763.RAHWGkXpdctBqftgKzqRDvlQqPUCTcn5Rjovi6bvkyJcg130_assertion wasDerivedFrom befree-2016 NP418763.RAHWGkXpdctBqftgKzqRDvlQqPUCTcn5Rjovi6bvkyJcg130_provenance.
- NP418763.RAHWGkXpdctBqftgKzqRDvlQqPUCTcn5Rjovi6bvkyJcg130_assertion wasGeneratedBy ECO_0000203 NP418763.RAHWGkXpdctBqftgKzqRDvlQqPUCTcn5Rjovi6bvkyJcg130_provenance.
- befree-2016 importedOn "2016-02-19" NP418763.RAHWGkXpdctBqftgKzqRDvlQqPUCTcn5Rjovi6bvkyJcg130_provenance.