Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1319097.RAHqS8X_cZ0mLCmeKI_Cyxl-V8HS4_mi-UbJDjBz70LDQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1319097.RAHqS8X_cZ0mLCmeKI_Cyxl-V8HS4_mi-UbJDjBz70LDQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1319097.RAHqS8X_cZ0mLCmeKI_Cyxl-V8HS4_mi-UbJDjBz70LDQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1319097.RAHqS8X_cZ0mLCmeKI_Cyxl-V8HS4_mi-UbJDjBz70LDQ130_provenance.
- NP1319097.RAHqS8X_cZ0mLCmeKI_Cyxl-V8HS4_mi-UbJDjBz70LDQ130_assertion description "[PASII/PMP22 and connexin 32 were also reported as target proteins of similar hereditary neuropathies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1319097.RAHqS8X_cZ0mLCmeKI_Cyxl-V8HS4_mi-UbJDjBz70LDQ130_provenance.
- NP1319097.RAHqS8X_cZ0mLCmeKI_Cyxl-V8HS4_mi-UbJDjBz70LDQ130_assertion evidence source_evidence_literature NP1319097.RAHqS8X_cZ0mLCmeKI_Cyxl-V8HS4_mi-UbJDjBz70LDQ130_provenance.
- NP1319097.RAHqS8X_cZ0mLCmeKI_Cyxl-V8HS4_mi-UbJDjBz70LDQ130_assertion SIO_000772 7706205 NP1319097.RAHqS8X_cZ0mLCmeKI_Cyxl-V8HS4_mi-UbJDjBz70LDQ130_provenance.
- NP1319097.RAHqS8X_cZ0mLCmeKI_Cyxl-V8HS4_mi-UbJDjBz70LDQ130_assertion wasDerivedFrom befree-2016 NP1319097.RAHqS8X_cZ0mLCmeKI_Cyxl-V8HS4_mi-UbJDjBz70LDQ130_provenance.
- NP1319097.RAHqS8X_cZ0mLCmeKI_Cyxl-V8HS4_mi-UbJDjBz70LDQ130_assertion wasGeneratedBy ECO_0000203 NP1319097.RAHqS8X_cZ0mLCmeKI_Cyxl-V8HS4_mi-UbJDjBz70LDQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP1319097.RAHqS8X_cZ0mLCmeKI_Cyxl-V8HS4_mi-UbJDjBz70LDQ130_provenance.