Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP818639.RADyeyywXFUp-vVGgmKPs8CW9oMaxOuljgOTug9X6ROlU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP818639.RADyeyywXFUp-vVGgmKPs8CW9oMaxOuljgOTug9X6ROlU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP818639.RADyeyywXFUp-vVGgmKPs8CW9oMaxOuljgOTug9X6ROlU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP818639.RADyeyywXFUp-vVGgmKPs8CW9oMaxOuljgOTug9X6ROlU130_provenance.
- NP818639.RADyeyywXFUp-vVGgmKPs8CW9oMaxOuljgOTug9X6ROlU130_assertion description "[Most cases of Rett syndrome (RTT) are caused by mutations in the methylated DNA-binding protein, MeCP2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP818639.RADyeyywXFUp-vVGgmKPs8CW9oMaxOuljgOTug9X6ROlU130_provenance.
- NP818639.RADyeyywXFUp-vVGgmKPs8CW9oMaxOuljgOTug9X6ROlU130_assertion evidence source_evidence_literature NP818639.RADyeyywXFUp-vVGgmKPs8CW9oMaxOuljgOTug9X6ROlU130_provenance.
- NP818639.RADyeyywXFUp-vVGgmKPs8CW9oMaxOuljgOTug9X6ROlU130_assertion SIO_000772 18499664 NP818639.RADyeyywXFUp-vVGgmKPs8CW9oMaxOuljgOTug9X6ROlU130_provenance.
- NP818639.RADyeyywXFUp-vVGgmKPs8CW9oMaxOuljgOTug9X6ROlU130_assertion wasDerivedFrom befree-20140225 NP818639.RADyeyywXFUp-vVGgmKPs8CW9oMaxOuljgOTug9X6ROlU130_provenance.
- NP818639.RADyeyywXFUp-vVGgmKPs8CW9oMaxOuljgOTug9X6ROlU130_assertion wasGeneratedBy ECO_0000203 NP818639.RADyeyywXFUp-vVGgmKPs8CW9oMaxOuljgOTug9X6ROlU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP818639.RADyeyywXFUp-vVGgmKPs8CW9oMaxOuljgOTug9X6ROlU130_provenance.