Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP859397.RAcUO4wSZpM2OJzPdg99Ncq6bdcUolDnYcItLCx4uucSk130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP859397.RAcUO4wSZpM2OJzPdg99Ncq6bdcUolDnYcItLCx4uucSk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP859397.RAcUO4wSZpM2OJzPdg99Ncq6bdcUolDnYcItLCx4uucSk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP859397.RAcUO4wSZpM2OJzPdg99Ncq6bdcUolDnYcItLCx4uucSk130_provenance.
- befree-2016 importedOn "2016-02-19" NP859397.RAcUO4wSZpM2OJzPdg99Ncq6bdcUolDnYcItLCx4uucSk130_provenance.
- NP859397.RAcUO4wSZpM2OJzPdg99Ncq6bdcUolDnYcItLCx4uucSk130_assertion wasGeneratedBy ECO_0000203 NP859397.RAcUO4wSZpM2OJzPdg99Ncq6bdcUolDnYcItLCx4uucSk130_provenance.
- NP859397.RAcUO4wSZpM2OJzPdg99Ncq6bdcUolDnYcItLCx4uucSk130_assertion wasDerivedFrom befree-2016 NP859397.RAcUO4wSZpM2OJzPdg99Ncq6bdcUolDnYcItLCx4uucSk130_provenance.
- NP859397.RAcUO4wSZpM2OJzPdg99Ncq6bdcUolDnYcItLCx4uucSk130_assertion SIO_000772 21160489 NP859397.RAcUO4wSZpM2OJzPdg99Ncq6bdcUolDnYcItLCx4uucSk130_provenance.
- NP859397.RAcUO4wSZpM2OJzPdg99Ncq6bdcUolDnYcItLCx4uucSk130_assertion evidence source_evidence_literature NP859397.RAcUO4wSZpM2OJzPdg99Ncq6bdcUolDnYcItLCx4uucSk130_provenance.
- NP859397.RAcUO4wSZpM2OJzPdg99Ncq6bdcUolDnYcItLCx4uucSk130_assertion description "[We investigated the chondroitin beta1,4-N-acetylgalactosaminyltransferase-1 (ChGn-1) gene in 114 patients affected with neuropathies including Guillain-Barré syndrome, chronic inflammatory demyelinating polyneuropathy, hereditary motor and sensory neuropathy (HMSN) and unknown etiology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP859397.RAcUO4wSZpM2OJzPdg99Ncq6bdcUolDnYcItLCx4uucSk130_provenance.