Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP340479.RAuWkjIXrqhYsQon9-2ZFBxarPRBDVWhxMtyAivgH_G6o130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP340479.RAuWkjIXrqhYsQon9-2ZFBxarPRBDVWhxMtyAivgH_G6o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP340479.RAuWkjIXrqhYsQon9-2ZFBxarPRBDVWhxMtyAivgH_G6o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP340479.RAuWkjIXrqhYsQon9-2ZFBxarPRBDVWhxMtyAivgH_G6o130_provenance.
- NP340479.RAuWkjIXrqhYsQon9-2ZFBxarPRBDVWhxMtyAivgH_G6o130_assertion description "[PME can be caused by the juvenile type of Gaucher's disease, which maps to chromosome 1q, by the juvenile type of neuronal ceroid lipofuscinoses (CLN3), which maps to chromosome 16p, and by the `cherry-red-spot-myoclonus` syndrome of Guazzi or sialidosis type I, which has been localized to chromosome 10.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP340479.RAuWkjIXrqhYsQon9-2ZFBxarPRBDVWhxMtyAivgH_G6o130_provenance.
- NP340479.RAuWkjIXrqhYsQon9-2ZFBxarPRBDVWhxMtyAivgH_G6o130_assertion evidence source_evidence_literature NP340479.RAuWkjIXrqhYsQon9-2ZFBxarPRBDVWhxMtyAivgH_G6o130_provenance.
- NP340479.RAuWkjIXrqhYsQon9-2ZFBxarPRBDVWhxMtyAivgH_G6o130_assertion SIO_000772 8293722 NP340479.RAuWkjIXrqhYsQon9-2ZFBxarPRBDVWhxMtyAivgH_G6o130_provenance.
- NP340479.RAuWkjIXrqhYsQon9-2ZFBxarPRBDVWhxMtyAivgH_G6o130_assertion wasDerivedFrom befree-20140225 NP340479.RAuWkjIXrqhYsQon9-2ZFBxarPRBDVWhxMtyAivgH_G6o130_provenance.
- NP340479.RAuWkjIXrqhYsQon9-2ZFBxarPRBDVWhxMtyAivgH_G6o130_assertion wasGeneratedBy ECO_0000203 NP340479.RAuWkjIXrqhYsQon9-2ZFBxarPRBDVWhxMtyAivgH_G6o130_provenance.
- befree-20140225 importedOn "2014-02-25" NP340479.RAuWkjIXrqhYsQon9-2ZFBxarPRBDVWhxMtyAivgH_G6o130_provenance.