Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1294835.RADJE2HQkZPGT670DFWzlPeEfpLKpWQ2zvpjxD9zMpZ0c130_assertion> ?p ?o ?g. }
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- NP1294835.RADJE2HQkZPGT670DFWzlPeEfpLKpWQ2zvpjxD9zMpZ0c130_assertion type Assertion NP1294835.RADJE2HQkZPGT670DFWzlPeEfpLKpWQ2zvpjxD9zMpZ0c130_head.
- NP1294835.RADJE2HQkZPGT670DFWzlPeEfpLKpWQ2zvpjxD9zMpZ0c130_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." NP1294835.RADJE2HQkZPGT670DFWzlPeEfpLKpWQ2zvpjxD9zMpZ0c130_provenance.
- NP1294835.RADJE2HQkZPGT670DFWzlPeEfpLKpWQ2zvpjxD9zMpZ0c130_assertion evidence source_evidence_literature NP1294835.RADJE2HQkZPGT670DFWzlPeEfpLKpWQ2zvpjxD9zMpZ0c130_provenance.
- NP1294835.RADJE2HQkZPGT670DFWzlPeEfpLKpWQ2zvpjxD9zMpZ0c130_assertion SIO_000772 26457357 NP1294835.RADJE2HQkZPGT670DFWzlPeEfpLKpWQ2zvpjxD9zMpZ0c130_provenance.
- NP1294835.RADJE2HQkZPGT670DFWzlPeEfpLKpWQ2zvpjxD9zMpZ0c130_assertion wasDerivedFrom befree-2016 NP1294835.RADJE2HQkZPGT670DFWzlPeEfpLKpWQ2zvpjxD9zMpZ0c130_provenance.
- NP1294835.RADJE2HQkZPGT670DFWzlPeEfpLKpWQ2zvpjxD9zMpZ0c130_assertion wasGeneratedBy ECO_0000203 NP1294835.RADJE2HQkZPGT670DFWzlPeEfpLKpWQ2zvpjxD9zMpZ0c130_provenance.