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- source_evidence_literature type ECO_0000212 NP195059.RAfOOkRf3jo1eX79H16q70qf-buNhSuBNAJc47jFIFswQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP195059.RAfOOkRf3jo1eX79H16q70qf-buNhSuBNAJc47jFIFswQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP195059.RAfOOkRf3jo1eX79H16q70qf-buNhSuBNAJc47jFIFswQ130_provenance.
- NP195059.RAfOOkRf3jo1eX79H16q70qf-buNhSuBNAJc47jFIFswQ130_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." NP195059.RAfOOkRf3jo1eX79H16q70qf-buNhSuBNAJc47jFIFswQ130_provenance.
- NP195059.RAfOOkRf3jo1eX79H16q70qf-buNhSuBNAJc47jFIFswQ130_assertion evidence source_evidence_literature NP195059.RAfOOkRf3jo1eX79H16q70qf-buNhSuBNAJc47jFIFswQ130_provenance.
- NP195059.RAfOOkRf3jo1eX79H16q70qf-buNhSuBNAJc47jFIFswQ130_assertion SIO_000772 8293722 NP195059.RAfOOkRf3jo1eX79H16q70qf-buNhSuBNAJc47jFIFswQ130_provenance.
- NP195059.RAfOOkRf3jo1eX79H16q70qf-buNhSuBNAJc47jFIFswQ130_assertion wasDerivedFrom befree-20140225 NP195059.RAfOOkRf3jo1eX79H16q70qf-buNhSuBNAJc47jFIFswQ130_provenance.
- NP195059.RAfOOkRf3jo1eX79H16q70qf-buNhSuBNAJc47jFIFswQ130_assertion wasGeneratedBy ECO_0000203 NP195059.RAfOOkRf3jo1eX79H16q70qf-buNhSuBNAJc47jFIFswQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP195059.RAfOOkRf3jo1eX79H16q70qf-buNhSuBNAJc47jFIFswQ130_provenance.