Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP807807.RAFqLMtyPC6WUR0xyIIOs8r17mGDrC-Uw9ZNVG9Uk6Kqw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP807807.RAFqLMtyPC6WUR0xyIIOs8r17mGDrC-Uw9ZNVG9Uk6Kqw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP807807.RAFqLMtyPC6WUR0xyIIOs8r17mGDrC-Uw9ZNVG9Uk6Kqw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP807807.RAFqLMtyPC6WUR0xyIIOs8r17mGDrC-Uw9ZNVG9Uk6Kqw130_provenance.
- NP807807.RAFqLMtyPC6WUR0xyIIOs8r17mGDrC-Uw9ZNVG9Uk6Kqw130_assertion description "[LGMD2H was mapped to a specific mutation in the TRIM32 gene and it has subsequently been shown that the same mutation also results in the `sarcotubular myopathy` syndrome, which was described histopathologically.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP807807.RAFqLMtyPC6WUR0xyIIOs8r17mGDrC-Uw9ZNVG9Uk6Kqw130_provenance.
- NP807807.RAFqLMtyPC6WUR0xyIIOs8r17mGDrC-Uw9ZNVG9Uk6Kqw130_assertion evidence source_evidence_literature NP807807.RAFqLMtyPC6WUR0xyIIOs8r17mGDrC-Uw9ZNVG9Uk6Kqw130_provenance.
- NP807807.RAFqLMtyPC6WUR0xyIIOs8r17mGDrC-Uw9ZNVG9Uk6Kqw130_assertion SIO_000772 21496629 NP807807.RAFqLMtyPC6WUR0xyIIOs8r17mGDrC-Uw9ZNVG9Uk6Kqw130_provenance.
- NP807807.RAFqLMtyPC6WUR0xyIIOs8r17mGDrC-Uw9ZNVG9Uk6Kqw130_assertion wasDerivedFrom befree-20140225 NP807807.RAFqLMtyPC6WUR0xyIIOs8r17mGDrC-Uw9ZNVG9Uk6Kqw130_provenance.
- NP807807.RAFqLMtyPC6WUR0xyIIOs8r17mGDrC-Uw9ZNVG9Uk6Kqw130_assertion wasGeneratedBy ECO_0000203 NP807807.RAFqLMtyPC6WUR0xyIIOs8r17mGDrC-Uw9ZNVG9Uk6Kqw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP807807.RAFqLMtyPC6WUR0xyIIOs8r17mGDrC-Uw9ZNVG9Uk6Kqw130_provenance.