Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP508918.RAAnOFaoewCqLR9bwB3WmyV7njLYRZTOveoJfbVkAuneU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP508918.RAAnOFaoewCqLR9bwB3WmyV7njLYRZTOveoJfbVkAuneU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP508918.RAAnOFaoewCqLR9bwB3WmyV7njLYRZTOveoJfbVkAuneU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP508918.RAAnOFaoewCqLR9bwB3WmyV7njLYRZTOveoJfbVkAuneU130_provenance.
- NP508918.RAAnOFaoewCqLR9bwB3WmyV7njLYRZTOveoJfbVkAuneU130_assertion description "[Subsequent progression of oligodendroglial tumors appears to be triggered by additional molecular features underlying the transition to anaplastic oligodendroglioma and glioblastoma multiforme (GBM) such as deletions of 9p and 10q, and alterations of CDKN2A (p16), which is located at 9p21.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP508918.RAAnOFaoewCqLR9bwB3WmyV7njLYRZTOveoJfbVkAuneU130_provenance.
- NP508918.RAAnOFaoewCqLR9bwB3WmyV7njLYRZTOveoJfbVkAuneU130_assertion evidence source_evidence_literature NP508918.RAAnOFaoewCqLR9bwB3WmyV7njLYRZTOveoJfbVkAuneU130_provenance.
- NP508918.RAAnOFaoewCqLR9bwB3WmyV7njLYRZTOveoJfbVkAuneU130_assertion SIO_000772 16102584 NP508918.RAAnOFaoewCqLR9bwB3WmyV7njLYRZTOveoJfbVkAuneU130_provenance.
- NP508918.RAAnOFaoewCqLR9bwB3WmyV7njLYRZTOveoJfbVkAuneU130_assertion wasDerivedFrom befree-2016 NP508918.RAAnOFaoewCqLR9bwB3WmyV7njLYRZTOveoJfbVkAuneU130_provenance.
- NP508918.RAAnOFaoewCqLR9bwB3WmyV7njLYRZTOveoJfbVkAuneU130_assertion wasGeneratedBy ECO_0000203 NP508918.RAAnOFaoewCqLR9bwB3WmyV7njLYRZTOveoJfbVkAuneU130_provenance.
- befree-2016 importedOn "2016-02-19" NP508918.RAAnOFaoewCqLR9bwB3WmyV7njLYRZTOveoJfbVkAuneU130_provenance.