Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP513957.RAnd5mbBuuvaWPwhSbgNaCeH1VB7aIhtOgT8L1Pd_q1hw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP513957.RAnd5mbBuuvaWPwhSbgNaCeH1VB7aIhtOgT8L1Pd_q1hw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP513957.RAnd5mbBuuvaWPwhSbgNaCeH1VB7aIhtOgT8L1Pd_q1hw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP513957.RAnd5mbBuuvaWPwhSbgNaCeH1VB7aIhtOgT8L1Pd_q1hw130_provenance.
- NP513957.RAnd5mbBuuvaWPwhSbgNaCeH1VB7aIhtOgT8L1Pd_q1hw130_assertion description "[We expressed mutants of MOG on human HeLa cells and analyzed sera from 111 patients (104 children, 7 adults) who recognized cell-bound human MOG, but had different diseases, including acute disseminated encephalomyelitis (ADEM), one episode of transverse myelitis or optic neuritis, multiple sclerosis (MS), anti-aquaporin-4 (AQP4)-negative neuromyelitis optica (NMO), and chronic relapsing inflammatory optic neuritis (CRION).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP513957.RAnd5mbBuuvaWPwhSbgNaCeH1VB7aIhtOgT8L1Pd_q1hw130_provenance.
- NP513957.RAnd5mbBuuvaWPwhSbgNaCeH1VB7aIhtOgT8L1Pd_q1hw130_assertion evidence source_evidence_literature NP513957.RAnd5mbBuuvaWPwhSbgNaCeH1VB7aIhtOgT8L1Pd_q1hw130_provenance.
- NP513957.RAnd5mbBuuvaWPwhSbgNaCeH1VB7aIhtOgT8L1Pd_q1hw130_assertion SIO_000772 24014878 NP513957.RAnd5mbBuuvaWPwhSbgNaCeH1VB7aIhtOgT8L1Pd_q1hw130_provenance.
- NP513957.RAnd5mbBuuvaWPwhSbgNaCeH1VB7aIhtOgT8L1Pd_q1hw130_assertion wasDerivedFrom befree-20140225 NP513957.RAnd5mbBuuvaWPwhSbgNaCeH1VB7aIhtOgT8L1Pd_q1hw130_provenance.
- NP513957.RAnd5mbBuuvaWPwhSbgNaCeH1VB7aIhtOgT8L1Pd_q1hw130_assertion wasGeneratedBy ECO_0000203 NP513957.RAnd5mbBuuvaWPwhSbgNaCeH1VB7aIhtOgT8L1Pd_q1hw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP513957.RAnd5mbBuuvaWPwhSbgNaCeH1VB7aIhtOgT8L1Pd_q1hw130_provenance.