Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP667051.RA6EAXL_NBaEvJOnD6t63zOlhZECFViZEgbnliA411p8Q130_assertion> ?p ?o ?g. }
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- NP667051.RA6EAXL_NBaEvJOnD6t63zOlhZECFViZEgbnliA411p8Q130_assertion type Assertion NP667051.RA6EAXL_NBaEvJOnD6t63zOlhZECFViZEgbnliA411p8Q130_head.
- NP667051.RA6EAXL_NBaEvJOnD6t63zOlhZECFViZEgbnliA411p8Q130_assertion description "[Therefore, on one hand our data confirm a role of driver mutations for copy number alterations (CNAs) included in the GBM genomic-signature (gain of chromosome 7- EGFR gene, loss of chromosome 13- RB1 gene, loss of chromosome 10-PTEN gene); on the other, it is not obvious that the new identified CNAs are passenger mutations, as they may be necessary for tumor progression specific for the individual patient.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP667051.RA6EAXL_NBaEvJOnD6t63zOlhZECFViZEgbnliA411p8Q130_provenance.
- NP667051.RA6EAXL_NBaEvJOnD6t63zOlhZECFViZEgbnliA411p8Q130_assertion evidence source_evidence_literature NP667051.RA6EAXL_NBaEvJOnD6t63zOlhZECFViZEgbnliA411p8Q130_provenance.
- NP667051.RA6EAXL_NBaEvJOnD6t63zOlhZECFViZEgbnliA411p8Q130_assertion SIO_000772 23468990 NP667051.RA6EAXL_NBaEvJOnD6t63zOlhZECFViZEgbnliA411p8Q130_provenance.
- NP667051.RA6EAXL_NBaEvJOnD6t63zOlhZECFViZEgbnliA411p8Q130_assertion wasDerivedFrom befree-20150227 NP667051.RA6EAXL_NBaEvJOnD6t63zOlhZECFViZEgbnliA411p8Q130_provenance.
- NP667051.RA6EAXL_NBaEvJOnD6t63zOlhZECFViZEgbnliA411p8Q130_assertion wasGeneratedBy ECO_0000203 NP667051.RA6EAXL_NBaEvJOnD6t63zOlhZECFViZEgbnliA411p8Q130_provenance.