Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP485970.RAtFfIjfMBcCo6lA34jPU65v85Fggy4nN7uN6ajuaX-qg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP485970.RAtFfIjfMBcCo6lA34jPU65v85Fggy4nN7uN6ajuaX-qg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP485970.RAtFfIjfMBcCo6lA34jPU65v85Fggy4nN7uN6ajuaX-qg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP485970.RAtFfIjfMBcCo6lA34jPU65v85Fggy4nN7uN6ajuaX-qg130_provenance.
- NP485970.RAtFfIjfMBcCo6lA34jPU65v85Fggy4nN7uN6ajuaX-qg130_assertion description "[Adenylosuccinate lyase (ADSL) deficiency (MIM 103050) is an autosomal recessive inborn error of purine synthesis characterized by the accumulation in body fluids of succinylaminoimidazolecarboxamide (SAICA) riboside and succinyladenosine (S-Ado), the dephosphorylated derivatives of the two substrates of the enzyme.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP485970.RAtFfIjfMBcCo6lA34jPU65v85Fggy4nN7uN6ajuaX-qg130_provenance.
- NP485970.RAtFfIjfMBcCo6lA34jPU65v85Fggy4nN7uN6ajuaX-qg130_assertion evidence source_evidence_literature NP485970.RAtFfIjfMBcCo6lA34jPU65v85Fggy4nN7uN6ajuaX-qg130_provenance.
- NP485970.RAtFfIjfMBcCo6lA34jPU65v85Fggy4nN7uN6ajuaX-qg130_assertion SIO_000772 10958654 NP485970.RAtFfIjfMBcCo6lA34jPU65v85Fggy4nN7uN6ajuaX-qg130_provenance.
- NP485970.RAtFfIjfMBcCo6lA34jPU65v85Fggy4nN7uN6ajuaX-qg130_assertion wasDerivedFrom befree-20140225 NP485970.RAtFfIjfMBcCo6lA34jPU65v85Fggy4nN7uN6ajuaX-qg130_provenance.
- NP485970.RAtFfIjfMBcCo6lA34jPU65v85Fggy4nN7uN6ajuaX-qg130_assertion wasGeneratedBy ECO_0000203 NP485970.RAtFfIjfMBcCo6lA34jPU65v85Fggy4nN7uN6ajuaX-qg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP485970.RAtFfIjfMBcCo6lA34jPU65v85Fggy4nN7uN6ajuaX-qg130_provenance.