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- source_evidence_literature type ECO_0000212 NP942460.RAptybwp-MB0Mh--0r_EXYagZ2R65gEB08wv_mL96DbyY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP942460.RAptybwp-MB0Mh--0r_EXYagZ2R65gEB08wv_mL96DbyY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP942460.RAptybwp-MB0Mh--0r_EXYagZ2R65gEB08wv_mL96DbyY130_provenance.
- NP942460.RAptybwp-MB0Mh--0r_EXYagZ2R65gEB08wv_mL96DbyY130_assertion description "[Exploring the potential role of disease-causing mutation in a gene desert: duplication of noncoding elements 5' of GRIA3 is associated with GRIA3 silencing and X-linked intellectual disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP942460.RAptybwp-MB0Mh--0r_EXYagZ2R65gEB08wv_mL96DbyY130_provenance.
- NP942460.RAptybwp-MB0Mh--0r_EXYagZ2R65gEB08wv_mL96DbyY130_assertion evidence source_evidence_literature NP942460.RAptybwp-MB0Mh--0r_EXYagZ2R65gEB08wv_mL96DbyY130_provenance.
- NP942460.RAptybwp-MB0Mh--0r_EXYagZ2R65gEB08wv_mL96DbyY130_assertion SIO_000772 22124977 NP942460.RAptybwp-MB0Mh--0r_EXYagZ2R65gEB08wv_mL96DbyY130_provenance.
- NP942460.RAptybwp-MB0Mh--0r_EXYagZ2R65gEB08wv_mL96DbyY130_assertion wasDerivedFrom befree-2016 NP942460.RAptybwp-MB0Mh--0r_EXYagZ2R65gEB08wv_mL96DbyY130_provenance.
- NP942460.RAptybwp-MB0Mh--0r_EXYagZ2R65gEB08wv_mL96DbyY130_assertion wasGeneratedBy ECO_0000203 NP942460.RAptybwp-MB0Mh--0r_EXYagZ2R65gEB08wv_mL96DbyY130_provenance.
- befree-2016 importedOn "2016-02-19" NP942460.RAptybwp-MB0Mh--0r_EXYagZ2R65gEB08wv_mL96DbyY130_provenance.