Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1311767.RAY5GTwsyaFcpXrYUw65r_nN2JwouRciTVjrLwssqydQI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1311767.RAY5GTwsyaFcpXrYUw65r_nN2JwouRciTVjrLwssqydQI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1311767.RAY5GTwsyaFcpXrYUw65r_nN2JwouRciTVjrLwssqydQI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1311767.RAY5GTwsyaFcpXrYUw65r_nN2JwouRciTVjrLwssqydQI130_provenance.
- NP1311767.RAY5GTwsyaFcpXrYUw65r_nN2JwouRciTVjrLwssqydQI130_assertion description "[Our findings are consistent with a novel molecular pathogenetic mechanism for myotonic dystrophy: both the normal and expanded DM kinase genes are transcribed in patient muscle, but the abnormal expansion-containing RNA has a dominant effect on RNA metabolism by preventing the accumulation of poly(A)+ RNA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1311767.RAY5GTwsyaFcpXrYUw65r_nN2JwouRciTVjrLwssqydQI130_provenance.
- NP1311767.RAY5GTwsyaFcpXrYUw65r_nN2JwouRciTVjrLwssqydQI130_assertion evidence source_evidence_literature NP1311767.RAY5GTwsyaFcpXrYUw65r_nN2JwouRciTVjrLwssqydQI130_provenance.
- NP1311767.RAY5GTwsyaFcpXrYUw65r_nN2JwouRciTVjrLwssqydQI130_assertion SIO_000772 7543316 NP1311767.RAY5GTwsyaFcpXrYUw65r_nN2JwouRciTVjrLwssqydQI130_provenance.
- NP1311767.RAY5GTwsyaFcpXrYUw65r_nN2JwouRciTVjrLwssqydQI130_assertion wasDerivedFrom befree-2016 NP1311767.RAY5GTwsyaFcpXrYUw65r_nN2JwouRciTVjrLwssqydQI130_provenance.
- NP1311767.RAY5GTwsyaFcpXrYUw65r_nN2JwouRciTVjrLwssqydQI130_assertion wasGeneratedBy ECO_0000203 NP1311767.RAY5GTwsyaFcpXrYUw65r_nN2JwouRciTVjrLwssqydQI130_provenance.
- befree-2016 importedOn "2016-02-19" NP1311767.RAY5GTwsyaFcpXrYUw65r_nN2JwouRciTVjrLwssqydQI130_provenance.