Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP925781.RAomUN7oyHsdtJHpmI_InpyQEzStUfj1tOryErYm0DePw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP925781.RAomUN7oyHsdtJHpmI_InpyQEzStUfj1tOryErYm0DePw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP925781.RAomUN7oyHsdtJHpmI_InpyQEzStUfj1tOryErYm0DePw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP925781.RAomUN7oyHsdtJHpmI_InpyQEzStUfj1tOryErYm0DePw130_provenance.
- NP925781.RAomUN7oyHsdtJHpmI_InpyQEzStUfj1tOryErYm0DePw130_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." NP925781.RAomUN7oyHsdtJHpmI_InpyQEzStUfj1tOryErYm0DePw130_provenance.
- NP925781.RAomUN7oyHsdtJHpmI_InpyQEzStUfj1tOryErYm0DePw130_assertion evidence source_evidence_literature NP925781.RAomUN7oyHsdtJHpmI_InpyQEzStUfj1tOryErYm0DePw130_provenance.
- NP925781.RAomUN7oyHsdtJHpmI_InpyQEzStUfj1tOryErYm0DePw130_assertion SIO_000772 11196669 NP925781.RAomUN7oyHsdtJHpmI_InpyQEzStUfj1tOryErYm0DePw130_provenance.
- NP925781.RAomUN7oyHsdtJHpmI_InpyQEzStUfj1tOryErYm0DePw130_assertion wasDerivedFrom befree-20140225 NP925781.RAomUN7oyHsdtJHpmI_InpyQEzStUfj1tOryErYm0DePw130_provenance.
- NP925781.RAomUN7oyHsdtJHpmI_InpyQEzStUfj1tOryErYm0DePw130_assertion wasGeneratedBy ECO_0000203 NP925781.RAomUN7oyHsdtJHpmI_InpyQEzStUfj1tOryErYm0DePw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP925781.RAomUN7oyHsdtJHpmI_InpyQEzStUfj1tOryErYm0DePw130_provenance.