Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1244291.RAqL1QF614GcX7UTCfgQ1vaxW_m12CXx8JatcA7FfhG_k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1244291.RAqL1QF614GcX7UTCfgQ1vaxW_m12CXx8JatcA7FfhG_k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1244291.RAqL1QF614GcX7UTCfgQ1vaxW_m12CXx8JatcA7FfhG_k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1244291.RAqL1QF614GcX7UTCfgQ1vaxW_m12CXx8JatcA7FfhG_k130_provenance.
- NP1244291.RAqL1QF614GcX7UTCfgQ1vaxW_m12CXx8JatcA7FfhG_k130_assertion description "[Mucopolysaccharidosis type VII (MPS VII, Sly syndrome) is a very rare lysosomal storage disease caused by a deficiency of the enzyme ?-glucuronidase (GUS), which is required for the degradation of three glycosaminoglycans (GAGs): dermatan sulfate, heparan sulfate, and chondroitin sulfate.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1244291.RAqL1QF614GcX7UTCfgQ1vaxW_m12CXx8JatcA7FfhG_k130_provenance.
- NP1244291.RAqL1QF614GcX7UTCfgQ1vaxW_m12CXx8JatcA7FfhG_k130_assertion evidence source_evidence_literature NP1244291.RAqL1QF614GcX7UTCfgQ1vaxW_m12CXx8JatcA7FfhG_k130_provenance.
- NP1244291.RAqL1QF614GcX7UTCfgQ1vaxW_m12CXx8JatcA7FfhG_k130_assertion SIO_000772 25468648 NP1244291.RAqL1QF614GcX7UTCfgQ1vaxW_m12CXx8JatcA7FfhG_k130_provenance.
- NP1244291.RAqL1QF614GcX7UTCfgQ1vaxW_m12CXx8JatcA7FfhG_k130_assertion wasDerivedFrom befree-2016 NP1244291.RAqL1QF614GcX7UTCfgQ1vaxW_m12CXx8JatcA7FfhG_k130_provenance.
- NP1244291.RAqL1QF614GcX7UTCfgQ1vaxW_m12CXx8JatcA7FfhG_k130_assertion wasGeneratedBy ECO_0000203 NP1244291.RAqL1QF614GcX7UTCfgQ1vaxW_m12CXx8JatcA7FfhG_k130_provenance.
- befree-2016 importedOn "2016-02-19" NP1244291.RAqL1QF614GcX7UTCfgQ1vaxW_m12CXx8JatcA7FfhG_k130_provenance.