Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP915767.RACCGQ68NjtxI0O6AMSzbCjXU2hmoVrJZWagRYCQmBiqM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP915767.RACCGQ68NjtxI0O6AMSzbCjXU2hmoVrJZWagRYCQmBiqM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP915767.RACCGQ68NjtxI0O6AMSzbCjXU2hmoVrJZWagRYCQmBiqM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP915767.RACCGQ68NjtxI0O6AMSzbCjXU2hmoVrJZWagRYCQmBiqM130_provenance.
- NP915767.RACCGQ68NjtxI0O6AMSzbCjXU2hmoVrJZWagRYCQmBiqM130_assertion description "[Mutations in peripheral myelin protein 22 (PMP22) can result in the common peripheral neuropathy Charcot-Marie-Tooth disease (CMTD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP915767.RACCGQ68NjtxI0O6AMSzbCjXU2hmoVrJZWagRYCQmBiqM130_provenance.
- NP915767.RACCGQ68NjtxI0O6AMSzbCjXU2hmoVrJZWagRYCQmBiqM130_assertion evidence source_evidence_literature NP915767.RACCGQ68NjtxI0O6AMSzbCjXU2hmoVrJZWagRYCQmBiqM130_provenance.
- NP915767.RACCGQ68NjtxI0O6AMSzbCjXU2hmoVrJZWagRYCQmBiqM130_assertion SIO_000772 21827951 NP915767.RACCGQ68NjtxI0O6AMSzbCjXU2hmoVrJZWagRYCQmBiqM130_provenance.
- NP915767.RACCGQ68NjtxI0O6AMSzbCjXU2hmoVrJZWagRYCQmBiqM130_assertion wasDerivedFrom befree-2016 NP915767.RACCGQ68NjtxI0O6AMSzbCjXU2hmoVrJZWagRYCQmBiqM130_provenance.
- NP915767.RACCGQ68NjtxI0O6AMSzbCjXU2hmoVrJZWagRYCQmBiqM130_assertion wasGeneratedBy ECO_0000203 NP915767.RACCGQ68NjtxI0O6AMSzbCjXU2hmoVrJZWagRYCQmBiqM130_provenance.
- befree-2016 importedOn "2016-02-19" NP915767.RACCGQ68NjtxI0O6AMSzbCjXU2hmoVrJZWagRYCQmBiqM130_provenance.