Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP712151.RAmwMtu2gFEMvrqNmkwlYee3lHAusCZlQ7SqH0Gue9BZU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP712151.RAmwMtu2gFEMvrqNmkwlYee3lHAusCZlQ7SqH0Gue9BZU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP712151.RAmwMtu2gFEMvrqNmkwlYee3lHAusCZlQ7SqH0Gue9BZU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP712151.RAmwMtu2gFEMvrqNmkwlYee3lHAusCZlQ7SqH0Gue9BZU130_provenance.
- NP712151.RAmwMtu2gFEMvrqNmkwlYee3lHAusCZlQ7SqH0Gue9BZU130_assertion description "[In this study, variation screening of the entire coding regions of CCR3 and CCR4 was performed, and possible association with several autoimmune diseases was tested, using the genomic DNA from 304 Japanese healthy individuals and 272 Japanese patients with rheumatic diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP712151.RAmwMtu2gFEMvrqNmkwlYee3lHAusCZlQ7SqH0Gue9BZU130_provenance.
- NP712151.RAmwMtu2gFEMvrqNmkwlYee3lHAusCZlQ7SqH0Gue9BZU130_assertion evidence source_evidence_literature NP712151.RAmwMtu2gFEMvrqNmkwlYee3lHAusCZlQ7SqH0Gue9BZU130_provenance.
- NP712151.RAmwMtu2gFEMvrqNmkwlYee3lHAusCZlQ7SqH0Gue9BZU130_assertion SIO_000772 11196669 NP712151.RAmwMtu2gFEMvrqNmkwlYee3lHAusCZlQ7SqH0Gue9BZU130_provenance.
- NP712151.RAmwMtu2gFEMvrqNmkwlYee3lHAusCZlQ7SqH0Gue9BZU130_assertion wasDerivedFrom befree-20140225 NP712151.RAmwMtu2gFEMvrqNmkwlYee3lHAusCZlQ7SqH0Gue9BZU130_provenance.
- NP712151.RAmwMtu2gFEMvrqNmkwlYee3lHAusCZlQ7SqH0Gue9BZU130_assertion wasGeneratedBy ECO_0000203 NP712151.RAmwMtu2gFEMvrqNmkwlYee3lHAusCZlQ7SqH0Gue9BZU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP712151.RAmwMtu2gFEMvrqNmkwlYee3lHAusCZlQ7SqH0Gue9BZU130_provenance.