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- source_evidence_literature type ECO_0000212 NP561780.RAwGOCTAxia2nrfw0vZHI_gEosnHRwnizHb2wpBS6ZRUA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP561780.RAwGOCTAxia2nrfw0vZHI_gEosnHRwnizHb2wpBS6ZRUA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP561780.RAwGOCTAxia2nrfw0vZHI_gEosnHRwnizHb2wpBS6ZRUA130_provenance.
- NP561780.RAwGOCTAxia2nrfw0vZHI_gEosnHRwnizHb2wpBS6ZRUA130_assertion description "[RSK4 is completely deleted in eight patients with the contiguous gene syndrome including MRX, partially deleted in a patient with DFN3 and present in patients with an Xq21 deletion and normal intellectual abilities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP561780.RAwGOCTAxia2nrfw0vZHI_gEosnHRwnizHb2wpBS6ZRUA130_provenance.
- NP561780.RAwGOCTAxia2nrfw0vZHI_gEosnHRwnizHb2wpBS6ZRUA130_assertion evidence source_evidence_literature NP561780.RAwGOCTAxia2nrfw0vZHI_gEosnHRwnizHb2wpBS6ZRUA130_provenance.
- NP561780.RAwGOCTAxia2nrfw0vZHI_gEosnHRwnizHb2wpBS6ZRUA130_assertion SIO_000772 10644430 NP561780.RAwGOCTAxia2nrfw0vZHI_gEosnHRwnizHb2wpBS6ZRUA130_provenance.
- NP561780.RAwGOCTAxia2nrfw0vZHI_gEosnHRwnizHb2wpBS6ZRUA130_assertion wasDerivedFrom befree-20140225 NP561780.RAwGOCTAxia2nrfw0vZHI_gEosnHRwnizHb2wpBS6ZRUA130_provenance.
- NP561780.RAwGOCTAxia2nrfw0vZHI_gEosnHRwnizHb2wpBS6ZRUA130_assertion wasGeneratedBy ECO_0000203 NP561780.RAwGOCTAxia2nrfw0vZHI_gEosnHRwnizHb2wpBS6ZRUA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP561780.RAwGOCTAxia2nrfw0vZHI_gEosnHRwnizHb2wpBS6ZRUA130_provenance.