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- source_evidence_literature type ECO_0000212 NP778984.RAG3_AnbRx6obU1v42YCPIPLzf-nvroTMoU1m4EfgP_nQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP778984.RAG3_AnbRx6obU1v42YCPIPLzf-nvroTMoU1m4EfgP_nQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP778984.RAG3_AnbRx6obU1v42YCPIPLzf-nvroTMoU1m4EfgP_nQ130_provenance.
- NP778984.RAG3_AnbRx6obU1v42YCPIPLzf-nvroTMoU1m4EfgP_nQ130_assertion description "[Thus, the unusual phenotypic features and mental retardation associated with the presence of a r(X) cannot be explained solely on the basis of presence or absence of XIST.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP778984.RAG3_AnbRx6obU1v42YCPIPLzf-nvroTMoU1m4EfgP_nQ130_provenance.
- NP778984.RAG3_AnbRx6obU1v42YCPIPLzf-nvroTMoU1m4EfgP_nQ130_assertion evidence source_evidence_literature NP778984.RAG3_AnbRx6obU1v42YCPIPLzf-nvroTMoU1m4EfgP_nQ130_provenance.
- NP778984.RAG3_AnbRx6obU1v42YCPIPLzf-nvroTMoU1m4EfgP_nQ130_assertion SIO_000772 15216549 NP778984.RAG3_AnbRx6obU1v42YCPIPLzf-nvroTMoU1m4EfgP_nQ130_provenance.
- NP778984.RAG3_AnbRx6obU1v42YCPIPLzf-nvroTMoU1m4EfgP_nQ130_assertion wasDerivedFrom befree-20150227 NP778984.RAG3_AnbRx6obU1v42YCPIPLzf-nvroTMoU1m4EfgP_nQ130_provenance.
- NP778984.RAG3_AnbRx6obU1v42YCPIPLzf-nvroTMoU1m4EfgP_nQ130_assertion wasGeneratedBy ECO_0000203 NP778984.RAG3_AnbRx6obU1v42YCPIPLzf-nvroTMoU1m4EfgP_nQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP778984.RAG3_AnbRx6obU1v42YCPIPLzf-nvroTMoU1m4EfgP_nQ130_provenance.