Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP308060.RAczXK4DMZbaPI9fRhfKqPREQ1HI_OPvbkP4f2KTGBKLo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP308060.RAczXK4DMZbaPI9fRhfKqPREQ1HI_OPvbkP4f2KTGBKLo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP308060.RAczXK4DMZbaPI9fRhfKqPREQ1HI_OPvbkP4f2KTGBKLo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP308060.RAczXK4DMZbaPI9fRhfKqPREQ1HI_OPvbkP4f2KTGBKLo130_provenance.
- NP308060.RAczXK4DMZbaPI9fRhfKqPREQ1HI_OPvbkP4f2KTGBKLo130_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." NP308060.RAczXK4DMZbaPI9fRhfKqPREQ1HI_OPvbkP4f2KTGBKLo130_provenance.
- NP308060.RAczXK4DMZbaPI9fRhfKqPREQ1HI_OPvbkP4f2KTGBKLo130_assertion evidence source_evidence_literature NP308060.RAczXK4DMZbaPI9fRhfKqPREQ1HI_OPvbkP4f2KTGBKLo130_provenance.
- NP308060.RAczXK4DMZbaPI9fRhfKqPREQ1HI_OPvbkP4f2KTGBKLo130_assertion SIO_000772 11196669 NP308060.RAczXK4DMZbaPI9fRhfKqPREQ1HI_OPvbkP4f2KTGBKLo130_provenance.
- NP308060.RAczXK4DMZbaPI9fRhfKqPREQ1HI_OPvbkP4f2KTGBKLo130_assertion wasDerivedFrom befree-2016 NP308060.RAczXK4DMZbaPI9fRhfKqPREQ1HI_OPvbkP4f2KTGBKLo130_provenance.
- NP308060.RAczXK4DMZbaPI9fRhfKqPREQ1HI_OPvbkP4f2KTGBKLo130_assertion wasGeneratedBy ECO_0000203 NP308060.RAczXK4DMZbaPI9fRhfKqPREQ1HI_OPvbkP4f2KTGBKLo130_provenance.
- befree-2016 importedOn "2016-02-19" NP308060.RAczXK4DMZbaPI9fRhfKqPREQ1HI_OPvbkP4f2KTGBKLo130_provenance.