Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP210057.RAImmiTcG_asS8YucU_zOLOvH_7pu9yRUQNLcFssHvIF0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP210057.RAImmiTcG_asS8YucU_zOLOvH_7pu9yRUQNLcFssHvIF0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP210057.RAImmiTcG_asS8YucU_zOLOvH_7pu9yRUQNLcFssHvIF0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP210057.RAImmiTcG_asS8YucU_zOLOvH_7pu9yRUQNLcFssHvIF0130_provenance.
- NP210057.RAImmiTcG_asS8YucU_zOLOvH_7pu9yRUQNLcFssHvIF0130_assertion description "[The expansion of CGG repeats in the 5'-untranslated region (5'UTR) of FMR1 gene is the molecular basis of fragile X syndrome in most of the patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP210057.RAImmiTcG_asS8YucU_zOLOvH_7pu9yRUQNLcFssHvIF0130_provenance.
- NP210057.RAImmiTcG_asS8YucU_zOLOvH_7pu9yRUQNLcFssHvIF0130_assertion evidence source_evidence_literature NP210057.RAImmiTcG_asS8YucU_zOLOvH_7pu9yRUQNLcFssHvIF0130_provenance.
- NP210057.RAImmiTcG_asS8YucU_zOLOvH_7pu9yRUQNLcFssHvIF0130_assertion SIO_000772 21499798 NP210057.RAImmiTcG_asS8YucU_zOLOvH_7pu9yRUQNLcFssHvIF0130_provenance.
- NP210057.RAImmiTcG_asS8YucU_zOLOvH_7pu9yRUQNLcFssHvIF0130_assertion wasDerivedFrom befree-20140225 NP210057.RAImmiTcG_asS8YucU_zOLOvH_7pu9yRUQNLcFssHvIF0130_provenance.
- NP210057.RAImmiTcG_asS8YucU_zOLOvH_7pu9yRUQNLcFssHvIF0130_assertion wasGeneratedBy ECO_0000203 NP210057.RAImmiTcG_asS8YucU_zOLOvH_7pu9yRUQNLcFssHvIF0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP210057.RAImmiTcG_asS8YucU_zOLOvH_7pu9yRUQNLcFssHvIF0130_provenance.