Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1222097.RAUhXqtff8Y6yOzdd3nWPVwBPvKzxbl7A2X8_Drf8atCU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1222097.RAUhXqtff8Y6yOzdd3nWPVwBPvKzxbl7A2X8_Drf8atCU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1222097.RAUhXqtff8Y6yOzdd3nWPVwBPvKzxbl7A2X8_Drf8atCU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1222097.RAUhXqtff8Y6yOzdd3nWPVwBPvKzxbl7A2X8_Drf8atCU130_provenance.
- NP1222097.RAUhXqtff8Y6yOzdd3nWPVwBPvKzxbl7A2X8_Drf8atCU130_assertion description "[Variants identified through this study were previously reported to be involved in FTD and/or MND, but we are the first to describe their effects as potential disease modifiers in the presence of a clear pathogenic mutation (i.e.C9ORF72 repeat expansion).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1222097.RAUhXqtff8Y6yOzdd3nWPVwBPvKzxbl7A2X8_Drf8atCU130_provenance.
- NP1222097.RAUhXqtff8Y6yOzdd3nWPVwBPvKzxbl7A2X8_Drf8atCU130_assertion evidence source_evidence_literature NP1222097.RAUhXqtff8Y6yOzdd3nWPVwBPvKzxbl7A2X8_Drf8atCU130_provenance.
- NP1222097.RAUhXqtff8Y6yOzdd3nWPVwBPvKzxbl7A2X8_Drf8atCU130_assertion SIO_000772 25239657 NP1222097.RAUhXqtff8Y6yOzdd3nWPVwBPvKzxbl7A2X8_Drf8atCU130_provenance.
- NP1222097.RAUhXqtff8Y6yOzdd3nWPVwBPvKzxbl7A2X8_Drf8atCU130_assertion wasDerivedFrom befree-2016 NP1222097.RAUhXqtff8Y6yOzdd3nWPVwBPvKzxbl7A2X8_Drf8atCU130_provenance.
- NP1222097.RAUhXqtff8Y6yOzdd3nWPVwBPvKzxbl7A2X8_Drf8atCU130_assertion wasGeneratedBy ECO_0000203 NP1222097.RAUhXqtff8Y6yOzdd3nWPVwBPvKzxbl7A2X8_Drf8atCU130_provenance.
- befree-2016 importedOn "2016-02-19" NP1222097.RAUhXqtff8Y6yOzdd3nWPVwBPvKzxbl7A2X8_Drf8atCU130_provenance.