Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1248047.RASIB5BSaFK0cS5EdrEneWWL5Td990OzPeGBQvPrYMkVk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1248047.RASIB5BSaFK0cS5EdrEneWWL5Td990OzPeGBQvPrYMkVk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1248047.RASIB5BSaFK0cS5EdrEneWWL5Td990OzPeGBQvPrYMkVk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1248047.RASIB5BSaFK0cS5EdrEneWWL5Td990OzPeGBQvPrYMkVk130_provenance.
- NP1248047.RASIB5BSaFK0cS5EdrEneWWL5Td990OzPeGBQvPrYMkVk130_assertion description "[Identification of a novel mutation in MAGT1 and progressive multifocal leucoencephalopathy in a 58-year-old man with XMEN disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1248047.RASIB5BSaFK0cS5EdrEneWWL5Td990OzPeGBQvPrYMkVk130_provenance.
- NP1248047.RASIB5BSaFK0cS5EdrEneWWL5Td990OzPeGBQvPrYMkVk130_assertion evidence source_evidence_literature NP1248047.RASIB5BSaFK0cS5EdrEneWWL5Td990OzPeGBQvPrYMkVk130_provenance.
- NP1248047.RASIB5BSaFK0cS5EdrEneWWL5Td990OzPeGBQvPrYMkVk130_assertion SIO_000772 25504528 NP1248047.RASIB5BSaFK0cS5EdrEneWWL5Td990OzPeGBQvPrYMkVk130_provenance.
- NP1248047.RASIB5BSaFK0cS5EdrEneWWL5Td990OzPeGBQvPrYMkVk130_assertion wasDerivedFrom befree-2016 NP1248047.RASIB5BSaFK0cS5EdrEneWWL5Td990OzPeGBQvPrYMkVk130_provenance.
- NP1248047.RASIB5BSaFK0cS5EdrEneWWL5Td990OzPeGBQvPrYMkVk130_assertion wasGeneratedBy ECO_0000203 NP1248047.RASIB5BSaFK0cS5EdrEneWWL5Td990OzPeGBQvPrYMkVk130_provenance.
- befree-2016 importedOn "2016-02-19" NP1248047.RASIB5BSaFK0cS5EdrEneWWL5Td990OzPeGBQvPrYMkVk130_provenance.