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- source_evidence_literature type ECO_0000212 NP1294834.RAXlqSc8B61hW3WeQ6iw3GocQOk3Q6TGKSmAINNKRboi0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1294834.RAXlqSc8B61hW3WeQ6iw3GocQOk3Q6TGKSmAINNKRboi0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1294834.RAXlqSc8B61hW3WeQ6iw3GocQOk3Q6TGKSmAINNKRboi0130_provenance.
- NP1294834.RAXlqSc8B61hW3WeQ6iw3GocQOk3Q6TGKSmAINNKRboi0130_assertion description "[Using Sanger sequencing, we determined the frequency of H3F3A, H3F3B, IDH1, and IDH2 mutations in GCTBs (n=60), chondroblastomas (n=12), and other giant cell-containing tumors (n=24), including aneurysmal bone cyst, chondromyxoid fibroma, and telangiectatic osteosarcoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1294834.RAXlqSc8B61hW3WeQ6iw3GocQOk3Q6TGKSmAINNKRboi0130_provenance.
- NP1294834.RAXlqSc8B61hW3WeQ6iw3GocQOk3Q6TGKSmAINNKRboi0130_assertion evidence source_evidence_literature NP1294834.RAXlqSc8B61hW3WeQ6iw3GocQOk3Q6TGKSmAINNKRboi0130_provenance.
- NP1294834.RAXlqSc8B61hW3WeQ6iw3GocQOk3Q6TGKSmAINNKRboi0130_assertion SIO_000772 26457357 NP1294834.RAXlqSc8B61hW3WeQ6iw3GocQOk3Q6TGKSmAINNKRboi0130_provenance.
- NP1294834.RAXlqSc8B61hW3WeQ6iw3GocQOk3Q6TGKSmAINNKRboi0130_assertion wasDerivedFrom befree-2016 NP1294834.RAXlqSc8B61hW3WeQ6iw3GocQOk3Q6TGKSmAINNKRboi0130_provenance.
- NP1294834.RAXlqSc8B61hW3WeQ6iw3GocQOk3Q6TGKSmAINNKRboi0130_assertion wasGeneratedBy ECO_0000203 NP1294834.RAXlqSc8B61hW3WeQ6iw3GocQOk3Q6TGKSmAINNKRboi0130_provenance.
- befree-2016 importedOn "2016-02-19" NP1294834.RAXlqSc8B61hW3WeQ6iw3GocQOk3Q6TGKSmAINNKRboi0130_provenance.