Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP568336.RAuOddPgoNRfd8sjbf4Xi39cYqLY8RK4vHcv7IOXzXtew130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP568336.RAuOddPgoNRfd8sjbf4Xi39cYqLY8RK4vHcv7IOXzXtew130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP568336.RAuOddPgoNRfd8sjbf4Xi39cYqLY8RK4vHcv7IOXzXtew130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP568336.RAuOddPgoNRfd8sjbf4Xi39cYqLY8RK4vHcv7IOXzXtew130_provenance.
- NP568336.RAuOddPgoNRfd8sjbf4Xi39cYqLY8RK4vHcv7IOXzXtew130_assertion description "[The MPZ role in the pathogenesis of both demyelinating and axonal inherited neuropathies was evaluated in the Italian population by screening a cohort of 214 patients with CMT1 or CMT2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP568336.RAuOddPgoNRfd8sjbf4Xi39cYqLY8RK4vHcv7IOXzXtew130_provenance.
- NP568336.RAuOddPgoNRfd8sjbf4Xi39cYqLY8RK4vHcv7IOXzXtew130_assertion evidence source_evidence_literature NP568336.RAuOddPgoNRfd8sjbf4Xi39cYqLY8RK4vHcv7IOXzXtew130_provenance.
- NP568336.RAuOddPgoNRfd8sjbf4Xi39cYqLY8RK4vHcv7IOXzXtew130_assertion SIO_000772 19293842 NP568336.RAuOddPgoNRfd8sjbf4Xi39cYqLY8RK4vHcv7IOXzXtew130_provenance.
- NP568336.RAuOddPgoNRfd8sjbf4Xi39cYqLY8RK4vHcv7IOXzXtew130_assertion wasDerivedFrom befree-20150227 NP568336.RAuOddPgoNRfd8sjbf4Xi39cYqLY8RK4vHcv7IOXzXtew130_provenance.
- NP568336.RAuOddPgoNRfd8sjbf4Xi39cYqLY8RK4vHcv7IOXzXtew130_assertion wasGeneratedBy ECO_0000203 NP568336.RAuOddPgoNRfd8sjbf4Xi39cYqLY8RK4vHcv7IOXzXtew130_provenance.
- befree-20150227 importedOn "2015-02-27" NP568336.RAuOddPgoNRfd8sjbf4Xi39cYqLY8RK4vHcv7IOXzXtew130_provenance.