Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1307125.RA0CBNhMTvsc9R7el6sRVe7rJbV4z7C1iLnCfFaDkaMsk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1307125.RA0CBNhMTvsc9R7el6sRVe7rJbV4z7C1iLnCfFaDkaMsk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1307125.RA0CBNhMTvsc9R7el6sRVe7rJbV4z7C1iLnCfFaDkaMsk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1307125.RA0CBNhMTvsc9R7el6sRVe7rJbV4z7C1iLnCfFaDkaMsk130_provenance.
- NP1307125.RA0CBNhMTvsc9R7el6sRVe7rJbV4z7C1iLnCfFaDkaMsk130_assertion description "[Although reduced acid beta-glucosidase activity appears to be the primary enzyme defect in type I Gaucher disease, patients with this disorder also have marked elevation of serum acid phosphatase and beta-hexosaminidase activities but with a normal level of lactic dehydrogenase activity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1307125.RA0CBNhMTvsc9R7el6sRVe7rJbV4z7C1iLnCfFaDkaMsk130_provenance.
- NP1307125.RA0CBNhMTvsc9R7el6sRVe7rJbV4z7C1iLnCfFaDkaMsk130_assertion evidence source_evidence_literature NP1307125.RA0CBNhMTvsc9R7el6sRVe7rJbV4z7C1iLnCfFaDkaMsk130_provenance.
- NP1307125.RA0CBNhMTvsc9R7el6sRVe7rJbV4z7C1iLnCfFaDkaMsk130_assertion SIO_000772 6859103 NP1307125.RA0CBNhMTvsc9R7el6sRVe7rJbV4z7C1iLnCfFaDkaMsk130_provenance.
- NP1307125.RA0CBNhMTvsc9R7el6sRVe7rJbV4z7C1iLnCfFaDkaMsk130_assertion wasDerivedFrom befree-2016 NP1307125.RA0CBNhMTvsc9R7el6sRVe7rJbV4z7C1iLnCfFaDkaMsk130_provenance.
- NP1307125.RA0CBNhMTvsc9R7el6sRVe7rJbV4z7C1iLnCfFaDkaMsk130_assertion wasGeneratedBy ECO_0000203 NP1307125.RA0CBNhMTvsc9R7el6sRVe7rJbV4z7C1iLnCfFaDkaMsk130_provenance.
- befree-2016 importedOn "2016-02-19" NP1307125.RA0CBNhMTvsc9R7el6sRVe7rJbV4z7C1iLnCfFaDkaMsk130_provenance.