Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1240811.RACzCvSLIGWJzK0B8nE21m1nl96P_-bQyXcWR-B6BdeD4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1240811.RACzCvSLIGWJzK0B8nE21m1nl96P_-bQyXcWR-B6BdeD4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1240811.RACzCvSLIGWJzK0B8nE21m1nl96P_-bQyXcWR-B6BdeD4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1240811.RACzCvSLIGWJzK0B8nE21m1nl96P_-bQyXcWR-B6BdeD4130_provenance.
- befree-2016 importedOn "2016-02-19" NP1240811.RACzCvSLIGWJzK0B8nE21m1nl96P_-bQyXcWR-B6BdeD4130_provenance.
- NP1240811.RACzCvSLIGWJzK0B8nE21m1nl96P_-bQyXcWR-B6BdeD4130_assertion wasGeneratedBy ECO_0000203 NP1240811.RACzCvSLIGWJzK0B8nE21m1nl96P_-bQyXcWR-B6BdeD4130_provenance.
- NP1240811.RACzCvSLIGWJzK0B8nE21m1nl96P_-bQyXcWR-B6BdeD4130_assertion wasDerivedFrom befree-2016 NP1240811.RACzCvSLIGWJzK0B8nE21m1nl96P_-bQyXcWR-B6BdeD4130_provenance.
- NP1240811.RACzCvSLIGWJzK0B8nE21m1nl96P_-bQyXcWR-B6BdeD4130_assertion SIO_000772 25430934 NP1240811.RACzCvSLIGWJzK0B8nE21m1nl96P_-bQyXcWR-B6BdeD4130_provenance.
- NP1240811.RACzCvSLIGWJzK0B8nE21m1nl96P_-bQyXcWR-B6BdeD4130_assertion evidence source_evidence_literature NP1240811.RACzCvSLIGWJzK0B8nE21m1nl96P_-bQyXcWR-B6BdeD4130_provenance.
- NP1240811.RACzCvSLIGWJzK0B8nE21m1nl96P_-bQyXcWR-B6BdeD4130_assertion description "[The most common CMT subtypes were CMT1A/PMP22 duplication, CMT1X/GJB1 mutation, CMT2A/MFN2 mutation, CMT1B/MPZ mutation, and hereditary neuropathy with liability to pressure palsy/PMP22 deletion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1240811.RACzCvSLIGWJzK0B8nE21m1nl96P_-bQyXcWR-B6BdeD4130_provenance.