Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP924876.RAf6iy5GGGm-4GLF7vGtcTBdyeM_snn2btwnrdWP1Gx-s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP924876.RAf6iy5GGGm-4GLF7vGtcTBdyeM_snn2btwnrdWP1Gx-s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP924876.RAf6iy5GGGm-4GLF7vGtcTBdyeM_snn2btwnrdWP1Gx-s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP924876.RAf6iy5GGGm-4GLF7vGtcTBdyeM_snn2btwnrdWP1Gx-s130_provenance.
- NP924876.RAf6iy5GGGm-4GLF7vGtcTBdyeM_snn2btwnrdWP1Gx-s130_assertion description "[As will be discussed in the manuscript, our work and reports by others from a normal population perspective support the hypothesis that individuals inheriting a GG genotype at position +49, for which lower CTLA4 expression has been extensively suggested, are more susceptible for developing autoimmune disorders and those with AA genotype, with an existence of a state of self-tolerance, may have a higher chance of developing cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP924876.RAf6iy5GGGm-4GLF7vGtcTBdyeM_snn2btwnrdWP1Gx-s130_provenance.
- NP924876.RAf6iy5GGGm-4GLF7vGtcTBdyeM_snn2btwnrdWP1Gx-s130_assertion evidence source_evidence_literature NP924876.RAf6iy5GGGm-4GLF7vGtcTBdyeM_snn2btwnrdWP1Gx-s130_provenance.
- NP924876.RAf6iy5GGGm-4GLF7vGtcTBdyeM_snn2btwnrdWP1Gx-s130_assertion SIO_000772 21931200 NP924876.RAf6iy5GGGm-4GLF7vGtcTBdyeM_snn2btwnrdWP1Gx-s130_provenance.
- NP924876.RAf6iy5GGGm-4GLF7vGtcTBdyeM_snn2btwnrdWP1Gx-s130_assertion wasDerivedFrom befree-2016 NP924876.RAf6iy5GGGm-4GLF7vGtcTBdyeM_snn2btwnrdWP1Gx-s130_provenance.
- NP924876.RAf6iy5GGGm-4GLF7vGtcTBdyeM_snn2btwnrdWP1Gx-s130_assertion wasGeneratedBy ECO_0000203 NP924876.RAf6iy5GGGm-4GLF7vGtcTBdyeM_snn2btwnrdWP1Gx-s130_provenance.
- befree-2016 importedOn "2016-02-19" NP924876.RAf6iy5GGGm-4GLF7vGtcTBdyeM_snn2btwnrdWP1Gx-s130_provenance.