Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP634803.RAqUaMYyferrzynGwGbn13sCHSKKa7jne0RrKV0J_9ZJw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP634803.RAqUaMYyferrzynGwGbn13sCHSKKa7jne0RrKV0J_9ZJw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP634803.RAqUaMYyferrzynGwGbn13sCHSKKa7jne0RrKV0J_9ZJw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP634803.RAqUaMYyferrzynGwGbn13sCHSKKa7jne0RrKV0J_9ZJw130_provenance.
- NP634803.RAqUaMYyferrzynGwGbn13sCHSKKa7jne0RrKV0J_9ZJw130_assertion description "[The defect, however, is different from I-cell disease and pseudo-Hurler polydystrophy, two disorders of post-translational lysosomal enzyme biosynthesis, since complementation studies demonstrated recovery of intracellular beta-galactosidase and alpha-neuraminidase levels in heterokaryons.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP634803.RAqUaMYyferrzynGwGbn13sCHSKKa7jne0RrKV0J_9ZJw130_provenance.
- NP634803.RAqUaMYyferrzynGwGbn13sCHSKKa7jne0RrKV0J_9ZJw130_assertion evidence source_evidence_literature NP634803.RAqUaMYyferrzynGwGbn13sCHSKKa7jne0RrKV0J_9ZJw130_provenance.
- NP634803.RAqUaMYyferrzynGwGbn13sCHSKKa7jne0RrKV0J_9ZJw130_assertion SIO_000772 7076257 NP634803.RAqUaMYyferrzynGwGbn13sCHSKKa7jne0RrKV0J_9ZJw130_provenance.
- NP634803.RAqUaMYyferrzynGwGbn13sCHSKKa7jne0RrKV0J_9ZJw130_assertion wasDerivedFrom befree-20140225 NP634803.RAqUaMYyferrzynGwGbn13sCHSKKa7jne0RrKV0J_9ZJw130_provenance.
- NP634803.RAqUaMYyferrzynGwGbn13sCHSKKa7jne0RrKV0J_9ZJw130_assertion wasGeneratedBy ECO_0000203 NP634803.RAqUaMYyferrzynGwGbn13sCHSKKa7jne0RrKV0J_9ZJw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP634803.RAqUaMYyferrzynGwGbn13sCHSKKa7jne0RrKV0J_9ZJw130_provenance.