Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP924876.RAf6iy5GGGm-4GLF7vGtcTBdyeM_snn2btwnrdWP1Gx-s130_assertion> ?p ?o ?g. }
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- NP924876.RAf6iy5GGGm-4GLF7vGtcTBdyeM_snn2btwnrdWP1Gx-s130_assertion type Assertion NP924876.RAf6iy5GGGm-4GLF7vGtcTBdyeM_snn2btwnrdWP1Gx-s130_head.
- 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.