Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP260346.RArGfUJGM_6IY8XMQAIpWSGHcqV5T6_x0CNXGFByV8pLM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP260346.RArGfUJGM_6IY8XMQAIpWSGHcqV5T6_x0CNXGFByV8pLM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP260346.RArGfUJGM_6IY8XMQAIpWSGHcqV5T6_x0CNXGFByV8pLM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP260346.RArGfUJGM_6IY8XMQAIpWSGHcqV5T6_x0CNXGFByV8pLM130_provenance.
- NP260346.RArGfUJGM_6IY8XMQAIpWSGHcqV5T6_x0CNXGFByV8pLM130_assertion description "[The presence of VCP mutations in patients with sporadic ALS, sporadic ALS-FTD, and progressive muscular atrophy (PMA), a known clinical mimic of inclusion body myopathy, is not known.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP260346.RArGfUJGM_6IY8XMQAIpWSGHcqV5T6_x0CNXGFByV8pLM130_provenance.
- NP260346.RArGfUJGM_6IY8XMQAIpWSGHcqV5T6_x0CNXGFByV8pLM130_assertion evidence source_evidence_literature NP260346.RArGfUJGM_6IY8XMQAIpWSGHcqV5T6_x0CNXGFByV8pLM130_provenance.
- NP260346.RArGfUJGM_6IY8XMQAIpWSGHcqV5T6_x0CNXGFByV8pLM130_assertion SIO_000772 22078486 NP260346.RArGfUJGM_6IY8XMQAIpWSGHcqV5T6_x0CNXGFByV8pLM130_provenance.
- NP260346.RArGfUJGM_6IY8XMQAIpWSGHcqV5T6_x0CNXGFByV8pLM130_assertion wasDerivedFrom befree-20140225 NP260346.RArGfUJGM_6IY8XMQAIpWSGHcqV5T6_x0CNXGFByV8pLM130_provenance.
- NP260346.RArGfUJGM_6IY8XMQAIpWSGHcqV5T6_x0CNXGFByV8pLM130_assertion wasGeneratedBy ECO_0000203 NP260346.RArGfUJGM_6IY8XMQAIpWSGHcqV5T6_x0CNXGFByV8pLM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP260346.RArGfUJGM_6IY8XMQAIpWSGHcqV5T6_x0CNXGFByV8pLM130_provenance.