Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP496500.RAcet5mar1YHLgBP3PPd64pMaM1jNNH6g4Wnw4O9ODlAc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP496500.RAcet5mar1YHLgBP3PPd64pMaM1jNNH6g4Wnw4O9ODlAc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP496500.RAcet5mar1YHLgBP3PPd64pMaM1jNNH6g4Wnw4O9ODlAc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP496500.RAcet5mar1YHLgBP3PPd64pMaM1jNNH6g4Wnw4O9ODlAc130_provenance.
- NP496500.RAcet5mar1YHLgBP3PPd64pMaM1jNNH6g4Wnw4O9ODlAc130_assertion description "[We genotyped six single-nucleotide polymorphisms (SNP) within or close to the IL5RA or IL5 genes in 82 patients with FIP1L1-PDGFRA-positive CEL plus, as controls, healthy individuals (n=100), patients with FIP1L1-PDGFRA-negative eosinophilia (n=100) or patients with chronic myeloid leukaemia (CML) (n=100).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP496500.RAcet5mar1YHLgBP3PPd64pMaM1jNNH6g4Wnw4O9ODlAc130_provenance.
- NP496500.RAcet5mar1YHLgBP3PPd64pMaM1jNNH6g4Wnw4O9ODlAc130_assertion evidence source_evidence_literature NP496500.RAcet5mar1YHLgBP3PPd64pMaM1jNNH6g4Wnw4O9ODlAc130_provenance.
- NP496500.RAcet5mar1YHLgBP3PPd64pMaM1jNNH6g4Wnw4O9ODlAc130_assertion SIO_000772 17914408 NP496500.RAcet5mar1YHLgBP3PPd64pMaM1jNNH6g4Wnw4O9ODlAc130_provenance.
- NP496500.RAcet5mar1YHLgBP3PPd64pMaM1jNNH6g4Wnw4O9ODlAc130_assertion wasDerivedFrom befree-20150227 NP496500.RAcet5mar1YHLgBP3PPd64pMaM1jNNH6g4Wnw4O9ODlAc130_provenance.
- NP496500.RAcet5mar1YHLgBP3PPd64pMaM1jNNH6g4Wnw4O9ODlAc130_assertion wasGeneratedBy ECO_0000203 NP496500.RAcet5mar1YHLgBP3PPd64pMaM1jNNH6g4Wnw4O9ODlAc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP496500.RAcet5mar1YHLgBP3PPd64pMaM1jNNH6g4Wnw4O9ODlAc130_provenance.