Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP607713.RAVcCvKF64wmO0BlNFIwgXNVSmMDFCb--Q4rPZq6lIBQ8130_assertion> ?p ?o ?g. }
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- NP607713.RAVcCvKF64wmO0BlNFIwgXNVSmMDFCb--Q4rPZq6lIBQ8130_assertion type Assertion NP607713.RAVcCvKF64wmO0BlNFIwgXNVSmMDFCb--Q4rPZq6lIBQ8130_head.
- NP607713.RAVcCvKF64wmO0BlNFIwgXNVSmMDFCb--Q4rPZq6lIBQ8130_assertion description "[To address these issues, we have investigated the MGMT methylation status, clinical and magnetic resonance imaging characteristics, and relevant genetic features (loss of heterozygosity on 17p and 19q, EGFR amplification, and p53 mutations) in a retrospective study on 86 patients affected by glioblastoma multiforme: 72 patients had a clinical history indicating de novo insurgence of the tumor and the remaining 14 were secondary glioblastoma multiforme.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP607713.RAVcCvKF64wmO0BlNFIwgXNVSmMDFCb--Q4rPZq6lIBQ8130_provenance.
- NP607713.RAVcCvKF64wmO0BlNFIwgXNVSmMDFCb--Q4rPZq6lIBQ8130_assertion evidence source_evidence_literature NP607713.RAVcCvKF64wmO0BlNFIwgXNVSmMDFCb--Q4rPZq6lIBQ8130_provenance.
- NP607713.RAVcCvKF64wmO0BlNFIwgXNVSmMDFCb--Q4rPZq6lIBQ8130_assertion SIO_000772 17473190 NP607713.RAVcCvKF64wmO0BlNFIwgXNVSmMDFCb--Q4rPZq6lIBQ8130_provenance.
- NP607713.RAVcCvKF64wmO0BlNFIwgXNVSmMDFCb--Q4rPZq6lIBQ8130_assertion wasDerivedFrom befree-2016 NP607713.RAVcCvKF64wmO0BlNFIwgXNVSmMDFCb--Q4rPZq6lIBQ8130_provenance.
- NP607713.RAVcCvKF64wmO0BlNFIwgXNVSmMDFCb--Q4rPZq6lIBQ8130_assertion wasGeneratedBy ECO_0000203 NP607713.RAVcCvKF64wmO0BlNFIwgXNVSmMDFCb--Q4rPZq6lIBQ8130_provenance.