Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP587168.RAR-9rRGi73MmnbAFZHoyMrnin1OVKPJZXyBleXwyeWd0130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP587168.RAR-9rRGi73MmnbAFZHoyMrnin1OVKPJZXyBleXwyeWd0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP587168.RAR-9rRGi73MmnbAFZHoyMrnin1OVKPJZXyBleXwyeWd0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP587168.RAR-9rRGi73MmnbAFZHoyMrnin1OVKPJZXyBleXwyeWd0130_provenance.
- NP587168.RAR-9rRGi73MmnbAFZHoyMrnin1OVKPJZXyBleXwyeWd0130_assertion description "[iPSC lines from patients with two distinct forms of axonal CMT (CMT2A and CMT2E) were differentiated into spinal cord motor neurons and used to study axonal structure and function and electrophysiological properties in vitro.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP587168.RAR-9rRGi73MmnbAFZHoyMrnin1OVKPJZXyBleXwyeWd0130_provenance.
- NP587168.RAR-9rRGi73MmnbAFZHoyMrnin1OVKPJZXyBleXwyeWd0130_assertion evidence source_evidence_literature NP587168.RAR-9rRGi73MmnbAFZHoyMrnin1OVKPJZXyBleXwyeWd0130_provenance.
- NP587168.RAR-9rRGi73MmnbAFZHoyMrnin1OVKPJZXyBleXwyeWd0130_assertion SIO_000772 25448007 NP587168.RAR-9rRGi73MmnbAFZHoyMrnin1OVKPJZXyBleXwyeWd0130_provenance.
- NP587168.RAR-9rRGi73MmnbAFZHoyMrnin1OVKPJZXyBleXwyeWd0130_assertion wasDerivedFrom befree-20150227 NP587168.RAR-9rRGi73MmnbAFZHoyMrnin1OVKPJZXyBleXwyeWd0130_provenance.
- NP587168.RAR-9rRGi73MmnbAFZHoyMrnin1OVKPJZXyBleXwyeWd0130_assertion wasGeneratedBy ECO_0000203 NP587168.RAR-9rRGi73MmnbAFZHoyMrnin1OVKPJZXyBleXwyeWd0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP587168.RAR-9rRGi73MmnbAFZHoyMrnin1OVKPJZXyBleXwyeWd0130_provenance.