Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP758568.RAQoOlEThjtpvjir-qwX7g_JLBm42CoaOXt51k52R7Nsg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP758568.RAQoOlEThjtpvjir-qwX7g_JLBm42CoaOXt51k52R7Nsg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP758568.RAQoOlEThjtpvjir-qwX7g_JLBm42CoaOXt51k52R7Nsg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP758568.RAQoOlEThjtpvjir-qwX7g_JLBm42CoaOXt51k52R7Nsg130_provenance.
- NP758568.RAQoOlEThjtpvjir-qwX7g_JLBm42CoaOXt51k52R7Nsg130_assertion description "[Mutations in the BIN1 gene cause centronuclear myopathy, which shares some histopathological features with myotonic dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP758568.RAQoOlEThjtpvjir-qwX7g_JLBm42CoaOXt51k52R7Nsg130_provenance.
- NP758568.RAQoOlEThjtpvjir-qwX7g_JLBm42CoaOXt51k52R7Nsg130_assertion evidence source_evidence_literature NP758568.RAQoOlEThjtpvjir-qwX7g_JLBm42CoaOXt51k52R7Nsg130_provenance.
- NP758568.RAQoOlEThjtpvjir-qwX7g_JLBm42CoaOXt51k52R7Nsg130_assertion SIO_000772 21623381 NP758568.RAQoOlEThjtpvjir-qwX7g_JLBm42CoaOXt51k52R7Nsg130_provenance.
- NP758568.RAQoOlEThjtpvjir-qwX7g_JLBm42CoaOXt51k52R7Nsg130_assertion wasDerivedFrom befree-20140225 NP758568.RAQoOlEThjtpvjir-qwX7g_JLBm42CoaOXt51k52R7Nsg130_provenance.
- NP758568.RAQoOlEThjtpvjir-qwX7g_JLBm42CoaOXt51k52R7Nsg130_assertion wasGeneratedBy ECO_0000203 NP758568.RAQoOlEThjtpvjir-qwX7g_JLBm42CoaOXt51k52R7Nsg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP758568.RAQoOlEThjtpvjir-qwX7g_JLBm42CoaOXt51k52R7Nsg130_provenance.