Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP543877.RAYy53iPGAMjobiwABF7dZh7bq6fhQDciubD18sm-48DQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP543877.RAYy53iPGAMjobiwABF7dZh7bq6fhQDciubD18sm-48DQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP543877.RAYy53iPGAMjobiwABF7dZh7bq6fhQDciubD18sm-48DQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP543877.RAYy53iPGAMjobiwABF7dZh7bq6fhQDciubD18sm-48DQ130_provenance.
- NP543877.RAYy53iPGAMjobiwABF7dZh7bq6fhQDciubD18sm-48DQ130_assertion description "[Autosomal-dominant centronuclear myopathy (CNM) due to mutations in the dynamin 2 gene (DNM2) is a rare congenital myopathy histopathologically characterized by centrally located nuclei and a radial arrangement of sarcoplasmic strands around the central nuclei.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP543877.RAYy53iPGAMjobiwABF7dZh7bq6fhQDciubD18sm-48DQ130_provenance.
- NP543877.RAYy53iPGAMjobiwABF7dZh7bq6fhQDciubD18sm-48DQ130_assertion evidence source_evidence_literature NP543877.RAYy53iPGAMjobiwABF7dZh7bq6fhQDciubD18sm-48DQ130_provenance.
- NP543877.RAYy53iPGAMjobiwABF7dZh7bq6fhQDciubD18sm-48DQ130_assertion SIO_000772 21221624 NP543877.RAYy53iPGAMjobiwABF7dZh7bq6fhQDciubD18sm-48DQ130_provenance.
- NP543877.RAYy53iPGAMjobiwABF7dZh7bq6fhQDciubD18sm-48DQ130_assertion wasDerivedFrom befree-20140225 NP543877.RAYy53iPGAMjobiwABF7dZh7bq6fhQDciubD18sm-48DQ130_provenance.
- NP543877.RAYy53iPGAMjobiwABF7dZh7bq6fhQDciubD18sm-48DQ130_assertion wasGeneratedBy ECO_0000203 NP543877.RAYy53iPGAMjobiwABF7dZh7bq6fhQDciubD18sm-48DQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP543877.RAYy53iPGAMjobiwABF7dZh7bq6fhQDciubD18sm-48DQ130_provenance.