Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP423087.RAas8u42kMvyL2mbEArDp5Hhy7R8lPRTTkVKndFs3vZl0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP423087.RAas8u42kMvyL2mbEArDp5Hhy7R8lPRTTkVKndFs3vZl0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP423087.RAas8u42kMvyL2mbEArDp5Hhy7R8lPRTTkVKndFs3vZl0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP423087.RAas8u42kMvyL2mbEArDp5Hhy7R8lPRTTkVKndFs3vZl0130_provenance.
- NP423087.RAas8u42kMvyL2mbEArDp5Hhy7R8lPRTTkVKndFs3vZl0130_assertion description "[We evaluated AQP4 expression relative to glial fibrillary acidic protein, extent of demyelination, lesion staging (CD68 staining for macrophages), and perivascular deposition of complement and immunoglobulin in 11 cases with NMO and NMO spectrum disorders (NMOSD), five with MS and 30 with other neurological diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP423087.RAas8u42kMvyL2mbEArDp5Hhy7R8lPRTTkVKndFs3vZl0130_provenance.
- NP423087.RAas8u42kMvyL2mbEArDp5Hhy7R8lPRTTkVKndFs3vZl0130_assertion evidence source_evidence_literature NP423087.RAas8u42kMvyL2mbEArDp5Hhy7R8lPRTTkVKndFs3vZl0130_provenance.
- NP423087.RAas8u42kMvyL2mbEArDp5Hhy7R8lPRTTkVKndFs3vZl0130_assertion SIO_000772 21241398 NP423087.RAas8u42kMvyL2mbEArDp5Hhy7R8lPRTTkVKndFs3vZl0130_provenance.
- NP423087.RAas8u42kMvyL2mbEArDp5Hhy7R8lPRTTkVKndFs3vZl0130_assertion wasDerivedFrom befree-20150227 NP423087.RAas8u42kMvyL2mbEArDp5Hhy7R8lPRTTkVKndFs3vZl0130_provenance.
- NP423087.RAas8u42kMvyL2mbEArDp5Hhy7R8lPRTTkVKndFs3vZl0130_assertion wasGeneratedBy ECO_0000203 NP423087.RAas8u42kMvyL2mbEArDp5Hhy7R8lPRTTkVKndFs3vZl0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP423087.RAas8u42kMvyL2mbEArDp5Hhy7R8lPRTTkVKndFs3vZl0130_provenance.