Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP779785.RAhrqWAtDXgK5PGs8o2zeB1i4mcqwlzVAyydgLfihupL0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP779785.RAhrqWAtDXgK5PGs8o2zeB1i4mcqwlzVAyydgLfihupL0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP779785.RAhrqWAtDXgK5PGs8o2zeB1i4mcqwlzVAyydgLfihupL0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP779785.RAhrqWAtDXgK5PGs8o2zeB1i4mcqwlzVAyydgLfihupL0130_provenance.
- NP779785.RAhrqWAtDXgK5PGs8o2zeB1i4mcqwlzVAyydgLfihupL0130_assertion description "[Immunohistochemical detection of C/EBP homologous protein (CHOP), immunoglobulin heavy chain binding protein (BiP), and hypoxia marker antigen D-110 in biopsies from three patients with MS primary or secondary progressive, three patients with clinically isolated syndrome, and one patient with lesional epilepsy was carried out.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP779785.RAhrqWAtDXgK5PGs8o2zeB1i4mcqwlzVAyydgLfihupL0130_provenance.
- NP779785.RAhrqWAtDXgK5PGs8o2zeB1i4mcqwlzVAyydgLfihupL0130_assertion evidence source_evidence_literature NP779785.RAhrqWAtDXgK5PGs8o2zeB1i4mcqwlzVAyydgLfihupL0130_provenance.
- NP779785.RAhrqWAtDXgK5PGs8o2zeB1i4mcqwlzVAyydgLfihupL0130_assertion SIO_000772 21382862 NP779785.RAhrqWAtDXgK5PGs8o2zeB1i4mcqwlzVAyydgLfihupL0130_provenance.
- NP779785.RAhrqWAtDXgK5PGs8o2zeB1i4mcqwlzVAyydgLfihupL0130_assertion wasDerivedFrom befree-20140225 NP779785.RAhrqWAtDXgK5PGs8o2zeB1i4mcqwlzVAyydgLfihupL0130_provenance.
- NP779785.RAhrqWAtDXgK5PGs8o2zeB1i4mcqwlzVAyydgLfihupL0130_assertion wasGeneratedBy ECO_0000203 NP779785.RAhrqWAtDXgK5PGs8o2zeB1i4mcqwlzVAyydgLfihupL0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP779785.RAhrqWAtDXgK5PGs8o2zeB1i4mcqwlzVAyydgLfihupL0130_provenance.