Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1065163.RAzpeX9C4yJkCYvz_2D_SFA7eXCTyYMU3LT4qXyikErFM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1065163.RAzpeX9C4yJkCYvz_2D_SFA7eXCTyYMU3LT4qXyikErFM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1065163.RAzpeX9C4yJkCYvz_2D_SFA7eXCTyYMU3LT4qXyikErFM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1065163.RAzpeX9C4yJkCYvz_2D_SFA7eXCTyYMU3LT4qXyikErFM130_provenance.
- befree-2016 importedOn "2016-02-19" NP1065163.RAzpeX9C4yJkCYvz_2D_SFA7eXCTyYMU3LT4qXyikErFM130_provenance.
- NP1065163.RAzpeX9C4yJkCYvz_2D_SFA7eXCTyYMU3LT4qXyikErFM130_assertion wasGeneratedBy ECO_0000203 NP1065163.RAzpeX9C4yJkCYvz_2D_SFA7eXCTyYMU3LT4qXyikErFM130_provenance.
- NP1065163.RAzpeX9C4yJkCYvz_2D_SFA7eXCTyYMU3LT4qXyikErFM130_assertion wasDerivedFrom befree-2016 NP1065163.RAzpeX9C4yJkCYvz_2D_SFA7eXCTyYMU3LT4qXyikErFM130_provenance.
- NP1065163.RAzpeX9C4yJkCYvz_2D_SFA7eXCTyYMU3LT4qXyikErFM130_assertion SIO_000772 23543484 NP1065163.RAzpeX9C4yJkCYvz_2D_SFA7eXCTyYMU3LT4qXyikErFM130_provenance.
- NP1065163.RAzpeX9C4yJkCYvz_2D_SFA7eXCTyYMU3LT4qXyikErFM130_assertion evidence source_evidence_literature NP1065163.RAzpeX9C4yJkCYvz_2D_SFA7eXCTyYMU3LT4qXyikErFM130_provenance.
- NP1065163.RAzpeX9C4yJkCYvz_2D_SFA7eXCTyYMU3LT4qXyikErFM130_assertion description "[Our results demonstrate that the TNPO3 mutation is the cause of limb-girdle muscular dystrophy 1F, expand our knowledge of the molecular basis of muscular dystrophies and bolster the importance of defects of nuclear envelope proteins as causes of inherited myopathies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1065163.RAzpeX9C4yJkCYvz_2D_SFA7eXCTyYMU3LT4qXyikErFM130_provenance.